The Stawinski Research Group

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Prof. Jacek Stawinski


 

Publication List 

 


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1975 - 1980  1981 - 1985  1986 - 1990  1991 - 1995  1996 - 2000   2001 - 2004   2005 -    


2005 - till present 


277. Stereoselective Methods for Carbon-Phosphorus (C–P) Bond Formation
in Stereoselective Synthesis of Drugs and Natural Products, Chapter 47, (ed.V. Andrushko and N. Andrushko), John Wiley & Sons Inc., 2012
M. Kalek and J. Stawinski
276. Computational Study of the Mechanism and Selectivity of Palladium-Catalyzed Propargylic Substitution with Phosphorus Nucleophiles
Chem. Eur. J., 18, 12424 – 12436 (2012)
J. O. Jimenez-Halla, M. Kalek, J. Stawinski, and F. Himo
275. Synthesis and QSAR study of novel cytotoxic spiro[3H-indole-3,2'(1'H)-pyrrolo [3,4-c]pyrrole] -2,3',5'(1H,2'aH,4'H)-triones
Eur. J. Med. Chem., 47, 312-322 (2012)
A. S. Girgis, J. Stawinski, N. S. Ismail, and H. Farag
274. DNA oligonucleotides with stereodefined phenylphosphonate and phosphonothioate internucleotide bonds: synthesis and physico-chemical properties
Arkivoc, 63-79 (2012)
M. Sobczak, T. Johansson, M. Bulkowski, M. Sochacki, G. Lavén, B. Mikolaczyk, J. Stawinski, and N. Nawrot
273. Nucleotide analogue, method of synthesis of nucleotide analogue, use of nucleotide analogue, aniviral peo.nucleotide, pharmaceutical composition
PCT WO 2912053917, 2012
A. Kraszewski, J. Romanowska, M. Sobkowski, A. Szymanska-Michalak, J. Stawinski, J. Boryski, A. Lipniacki, and A. Piasek
272. Novel, Stereoselective and Stereospecific Synthesis of Allenylphosphonates and Related Compounds via Palladium-Catalyzed Propargylic Substitution
Adv. Synth. Cat., 353, 1741-1755 (2011)
M. Kalek and J. Stawinski
271. Aryl H-Phosphonates 17: (N-Aryl)phosphoramidates of Pyrimidine Nucleoside Analogues and Their Synthesis, Selected Properties, and Anti-HIV Activity
J. Med. Chem., 54, 6482-6491 (2011)
J. Romanowska, M. Sobkowski, A. Szymanska-Michalak, K. Kolodziej, A. Dabrowska, A. Lipniacki, A. Piasek, Z. M. Pietrusiewicz, M. Figlerowicz, A. Guranowski, J. Boryski, J. Stawinski, and A. Kraszewski
270. 31P NMR and Computational Studies on Stereochemistry of Conversion of Phosphoramidate Diesters into the Corresponding Phosphotriesters
Nucleosides, Nucleotides, Nucleic Acids, 30, 552-564 (2011)
L. Söderberg, G. Lavén, M. Kalek, and J. Stawinski
269. Unusual stereochemistry of esterification of uridine 3'-H-phosphonothioate
Phosphor. Sulfur Silicon, 186, 952-955 (2011)
M. Sobkowski, J. Stawinski, and A. Kraszewski
268. Palladium-catalyzed propargylic substitution with phosphorus nucleophiles:efficient, stereoselective synhtesis of allenylphosphonates adn related compounds
Org. Lett., 12,  4702-4704 (2010)
M. Kalek, T. Johansson, M. Jezowska, J. Stawinski
267. Studies on the decomposition pathways of diastereoisomeric mixtures of aryl nucleoside a-hydroxyphosphonates under hydrolytic conditions. Synthesis of a-hydroxyphosphonate monoesters
New J. Chem., 34, 976-983 (2010)
A. Szymanska-Michalak, J. Stawinski, and A. Kraszewski
266. O-Silylated C3-halohydrins as a novel class of protected building blocks for total, regio- and stereocontrolled synthesis of glycerolipid frameworks
Org. Biomol. Chem., 8, 463-477 (2010)
S. D. Stamatov and J. Stawinski
265. Stereochemistry of Internucleotide Bond Formation by the H-Phosphonate Method.  5.  The Role of Brønsted and H-Bonding Base Catalysis in Ribonucleoside H-Phosphonate Condensation – Chemical and Stereochemical Consequences
Nucleos. Nucleot. Nucl. Acids, 29, 628–645 (2010)
M. Sobkowski, J. Stawinski, and A. Kraszewski
264. Stereochemistry of internucleotide bond formation by the H-phosphonate method. 7. Stereoselective formation of ribonucleoside (RP)- and (SP)-3'-O-H-phosphonothioate monoesters
Tetrahedron Asymm., 21, 410-419 (2010)
M. Sobkowski, J. Stawinski, and A. Kraszewski
263. Preparation of benzylphosphonates via a palladium(0)-catalyzed cross-coupling of H-phosphonate diesters with benzyl halides. Synthetic and mechanistic studies
New J. Chem., 34, 967-975 (2010)
G. Laven, M. Kalek, M. Jezowska, and J. Stawinski
262. Palladium-catalyzed propargylic substitution with phosphorus nucleophiles
Am. Chem. Soc. Meeting, Abstracts of Papers, ORGN-487 (2010)
M. Kalek, M. Jezowska, and J. Stawinski
261. On the Sulfurization of H-Phosphonate Diesters and Phosphite Triesters Using Elemental Sulfur
Phosphorus, Sulfur, and Silicon, 184, 908-916 (2009)
R. Wallin, M. Kalek, A. Bartoszewicz, M. Thelin, and J. Stawinski
260. The role of nucleophilic catalysis in chemistry and stereochemistry of ribonucleoside H-phosphonate condensation
New J. Chem., 33, 164-170 (2009)
M. Sobkowski, J. Stawinski, and A. Kraszewski
259. A proposal for a convenient notation for P-chiral nucleotide analogues. Part 4. A relationship between the Dp/Lp notation and stereochemistry of reactions
Nucleos. Nucleot. Nucl. Acids, 28, 29-42 (2009)
M. Sobkowski, J. Stawinski, and A. Kraszewski
258. A New, Efficient Entry to Non-Lipophilic H-Phosphonate Monoesters – Preparation of Anti-HIV Nucleotide Analogues
Lett. Org. Chem., 6, 496-499 (2009)
J. Romanowska, A. Szymańska-Michalak, M. Pietkiewicz, M. Sobkowski, J. Boryski, J. Stawinski, and A. Kraszewski
257. Aryl nucleoside H-phosphonates. Part 16: Synthesis and anti-HIV-1 activity of di-aryl nucleoside phosphotriesters
Bioorg. Med. Chem., 17, 3489-3498 (2009)
J. Romanowska, A. Szymanska-Michalak, J. Boryski, J. Stawinski, A. Kraszewski, R. Loddo, G. Sanna, G. Collu, B. Secci, and P. La Colla
256. Palladium(0)-Catalyzed Benzylation of H-Phosphonate Diesters: An Efficient Entry to Benzylphosphonates
Synlett, 225-228 (2009)
G. Lavén and J. Stawinski
255. Synthetic studies on the preparation of nucleoside 5′-H-phosphonate monoesters under the Mitsunobu reaction conditions
Arkivoc, 20-27 (2009)
G. Lavén and J. Stawinski
254. Efficient synthesis of mono- and diarylphosphinic acids: a microwave-assisted palladium-catalyzed cross-coupling of aryl halides with phosphinate
Tetrahedron, 65, 10406–10412 (2009)
M. Kalek and J. Stawinski
253. Preparation of Arylphosphonates by Palladium(0)-Catalyzed Cross-Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic Studies
Adv. Synth. Catal., 351, 3207-3216 (2009)
M. Kalek, M. Jezowska, and J. Stawinski
252. Regioselective and Stereospecific Halosilylating Cleavage of the Oxirane System of Glycidol Derivatives as an Efficient Strategy to C2-O-Functionalized C3-Vicinal Halohydrins
Eur. J. Org. Chem., 2635-2643 (2008)
S. D. Stamatov and J. Stawinski
251. Stereochemistry of internucleotide bond formation by the H-phosphonate method. Part 6: Optimization of the reaction conditions towards highest stereoselectivity
Tetrahedron Asymm., 19, 2508-2518 (2008)
M. Sobkowski, J. Stawinski, and A. Kraszewski
250. A new synthetic route to diastereomerically pure P-chiral nucleotide analogues, dinucleoside benzylphosphonates, via stereospecific Pd(0) catalyzed cross-coupling reaction
Collection Symposium Series, 10, 395-397 (2008)
G. Lavén and J. Stawinski
249. Microwave-Assisted Palladium-Catalyzed Cross-Coupling of Aryl and Vinyl Halides with H-Phosphonate Diesters
Org. Lett., 10, 4637-4640 (2008)
M. Kalek, A. Ziadi, and J. Stawinski
248. Palladium-Catalyzed C-P Bond Formation: Mechanistic Studies on the Ligand Substitution and the Reductive Elimination. An Intramolecular Catalysis by the Acetate Group in Pd(II) Complexes
Organometallics, 27, 5876-5888 (2008)
M. Kalek and J. Stawinski
247. Synthetic studies on the P-C bond formation via a palladium-catalyzed cross-coupling reaction. Application to the synthesis of P-arylated nucleic acids.
Collection Symposium Series, 10, 214-218 (2008)
M. Kalek and J. Stawinski
246. Synthesis of nucleoside phosphorothio-, phosphorodithio- and phosphoroselenoate diesters via oxidative esterification of the corresponding H-phosphonate analogues
Nucleic Acids Sym. Ser., 52, 285-286 (2008)
M. Kalek, A. Bartoszewicz, and J. Stawinski
245. Iodine-promoted silylation of alcohols with silyl chlorides. Synthetic and mechanistic studies
Tetrahedron, 64, 8843-8850 (2008)
A. Bartoszewicz, M. Kalek, and J. Stawinski
244. The case for the intermediacy of monomeric metaphosphate analogues during oxidation of H-phosphonothioate, H-phosphonodithioate, and H-phosphonoselenoate monoesters: Mechanistic and synthetic studies
J. Org. Chem., 73, 5029-5038 (2008)
A. Bartoszewicz, M. Kalek, and J. Stawinski
243. Synthesis of nucleoside phosphorothio-, phosphorodithio- and phosphoroselenoate diesters via oxidative esterification of the corresponding H-phosphonate analogues
Collection Symposium Series, 10, 219-223 (2008)
A. Bartoszewicz, M. Kalek, and J. Stawinski
242. A New Reagent System for Efficient Silylation of Alcohols: Silyl Chloride– N-Methylimidazole–Iodine
Synlett, 37-40 (2008)
A. Bartoszewicz, M. Kalek, J. Nilsson, R. Hiresova, and J. Stawinski
241. Regioselective and stereospecific acylation across oxirane- and silyloxy systems as a novel strategy to the synthesis of enantiomerically pure mono-, di- and triglycerides
Org. Biomol. Chem., 5, 3787-3800 (2007)
S. D. Stamatov and J. Stawinski
240. Regioselective and stereospecific opening of an oxirane system mediated by trifluoroacetic acid and halide anions. A new direct approach to C3-vicinal halohydrins
Tetrahedron Lett., 48, 1887-1889 (2007)
S. D. Stamatov and J. Stawinski
239. Direct Trifluoroacetylation Across a Trimethylsilyloxy System as a Stereospecific, Chemo- and Regioselective Approach to C3-Vicinal Halohydrins
Synlett, 439-442 (2007)
S. D. Stamatov and J. Stawinski
238. A Convenient Stereochemical Notation for P-Chiral Nucleotide Analogs
In: Current Protocols in Nucleic Acid Chemistry, ed. S. L. Beaucage, D. E. Bergstrom, G. D. Glick and R. A. Jones, John Wiley & Sons, Inc., New York, p. Appendix 1E, p. A.1E1-A.1E16 (2007)
M. Sobkowski, J. Stawinski, and A. Kraszewski
237. Stereochemistry of internucleotide bond formation by the H-phosphonate method. Part 3: Investigations on a mechanism of asymmetric induction
Tetrahedron Asymm., 18, 2336-2348 (2007)
M. Sobkowski, A. Kraszewski, and J. Stawinski
236. H-Phosphonates: Versatile synthetic precursors to biologically active phosphorus compounds
Pure & Appl. Chem., 79, 2217-2227 (2007)
A. Kraszewski and J. Stawinski
235. Pd(0)-Catalyzed Phosphorus-Carbon Bond Formation. Mechanistic and Synthetic Studies on the Role of the Palladium Sources and Anionic Additives
Organometallics, 26, 5840-5847 (2007)
M. Kalek and J. Stawinski
234. Nucleoside H-Phosphonates, XXII: Synthesis and Properties of New Nucleotide Analogues – H-Phosphonothiolate Diesters
Synlett, 2748-2752 (2007)
R. Hiresova and J. Stawinski
233. Studies on the condensation of H-phoshonate monoesters with S-nucleophiles
Am. Chem. Soc. Meeting, Abstracts of Papers, ORGN-161 (2007)
R. Hiresova and J. Stawinski
232. A proposal for a convenient notation for P-chiral nucleotide analogues. Part 3. Compounds with one nucleoside residue and non-nuclesidic derivatives
Nucleosides Nucleotides Nucleic Acids 25, 1377-1389 (2006)
M. Sobkowski, J. Stawinski, and A. Kraszewski
231. A proposal for a convenient notation for P-chiral nucleotide analogues. Part 2. Dinucleoside monophosphoate analogues
Nucleosides Nucleotides Nucleic Acids 25, 1368-1375 (2006)
M. Sobkowski, J. Stawinski, and A. Kraszewski
230. Preparation of oligodeoxyribonucleotide phosphorothioates via intramolecular and intermolecular nucleophilic substitution using protecting group catalysis conditions
PCT Int. Appl. (2006), 67 pp. WO 2006066260
T. Szabo and J. Stawinski
229.
Regioselective, Haloacylating Cleavage of an Oxirane System Mediated by Trifluoroacetic Anhydride/Trimethylsilyl Halides: An Efficient Entry to 2-Acyl-3-haloglycerols
Synlett, 2251-2255 (2006)
S. D. Stamatov and J. Stawinski
228. The influences of a nitrogen atom position in dinucleoside 2-,3-,4-pyridylphosphonates on fragmentation patterns in electrospray ionization multistage tandem mass spectra
Nucleosides Nucleotides Nucleic Acids, 25, 771-784 (2006)
S. H. Ji, Y. Ju, H. Fu, Y. F. Zhao, T. Johansson, and J. Stawinski
227.    Regioselective and stereospecific cleavage of a terminal oxirane system: A novel synthetic approach to lipid mediator 1,2(2,3)-diacyl-3(1)-halo-sn-glycerols
Bioorg. Med. Chem. Lett., 16, 3388-3391 (2006)
S. D. Stamatov and J. Stawinski
226.
Aryl nucleoside H-phosphonates. Part 15: Synthesis, properties and, anti-HIV activity of aryl nucleoside 5'-0-a-hydroxyphosphonates
Bioorg. Med. Chem., 14, 1924-1934 (2006)
A. Szymanska, M. Szymczak, J. Boryski, J. Stawinski, A. Kraszewski, G. Collu, G. Sanna, G. Giliberti, R. Loddob, and  P. La Colla
225.
Efficient, highly regioselective, and stereospecific conversion of glycidol systems into C2-O-acylated vicinal halohydrins
Tetrahedron Lett., 47, 2543-2547 (2006)
S. D. Stamatov and J. Stawinski
224.
Nucleoside H-phosphonates. XXI. Synthetic and 31P NMR studie on the preparation of dinucleoside H-phosphonoselenoates
Coll. Czech. Chem. Commun., 71, 820-831 (2006)
M. Kullberg, M. Bollmark, and J. Stawinski
223.
Studies on oxidative  transformations of dinucleoside H-phosphonoselenoates
Coll. Czech. Chem. Commun., 71, 832-841 (2006)
M. Bollmark, M. Kullberg, and J. Stawinski
222. Direct Acylation across a Silyloxy System of Glycerol with Carboxylic Acid Anhydrides: A Novel Strategy  to the Prodrug Carrier Modules 1,3-     Diacylsn- glycerols
Synlett, 2587-2590 (2005)
S. D. Stamatov and J. Stawinski
221. A direct transformation of O-silyl groups into O-trichloroacetates. A novel synthetic approach to protein kinase C ligands: 1-oleoyl-2-acetyl-  and 1-hexadecyl-2-acetyl-sn-glycerols
Tetrahedron Lett., 46, 6855-6859 (2005)
S. D. Stamatov, M. Kullberg, and J. Stawinski
220. A proposal of Dp/Lp notation for nucleotide analogues with a chiral phosphorus centre
Collection Symposium Series, 7, 467-469 (2005)
M. Sobkowski, J. Stawinski, and A. Kraszewski
219. Stereochemistry of internucleotide bond formation by the H-phosphonate method. 2. Transesterification of aryl ribonucleoside H- phosphonate diesters with alcohols
Collection Symposium Series, 7, 183-187 (2005)
M. Sobkowski, J. Jankowska, J. Stawinski, and A. Kraszewski
218. Stereochemistry of internucleotide bond formation by the H-phosphonate method. 1. Synthesis and 31P NMR analysis of 16 diribonucleoside (3'-5')-H-phosphonates adn the corresponding phosphorothioates
Nucleos. Nucleot. Nucl. Acids, 24, 1469-1484 (2005)
M. Sobkowski, J. Jankowska, A. Kraszewski, and J. Stawinski
217. Developing synthetic methods for bioactive phosphorus compounds. A progress report
Collection Symposium Series, 7, 189-193 (2005)
J. Nilsson, T. Szabo, G. Lavén, A. Kraszewski, and J. Stawinski
216. Synthetic studies on the preparation of dinucleoside phenylphosphonates and dinucleoside phenylphosphonothioates via palladium(0)  catalysed cross-coupling
Collection Symposium Series, 7, 195-199 (2005)
G. Lavén and J. Stawinski
215. Reaction of H-phosphonate and H-phosphonothioate diesters with carbonyl compounds. 31P NMR studies
Collection Symposium Series, 7, 207-211 (2005)
M. Kullberg and J. Stawinski
214. Determination of absolute configuration of nucleoside 3’-H-phosphonothioate monoesters via stereochemical correlation  analysis
Collection Symposium Series, 7, 201-205 (2005)
R. Hiresova, L. Putilova, M. Kullberg, and J. Stawinski
213. Theoretical investigations on the mechanism of chalcogens exchange reaction between P(V) and P(III) compounds
Organomet. Chem., 690, 2571-2576 (2005)
M. Kullberg and J. Stawinski
212. A proposal for a new stereochemical notation for P-chiral nucleotide analogues and related compounds
Nucleos. Nucleot. Nucl. Acids, 24, 1301-1307  (2005)
M. Sobkowski, J. Stawinski, and A. Kraszewski
211. Nucleoside H-Phosphonates XX. Efficient Method for the Preparation of Nucleoside H-Phosphonoselenoate Monoesters
Synthesis, 1668-1674 (2005)
M. Kullberg and J. Stawinski
210. Preparation of Nucleoside H-Phosphonoselenoate Monoesters via the Phosphinate Approach
Nucleos. Nucleot. Nucl. Acids, 24, 1627-1633  (2005)
M. Kullberg and J. Stawinski
209. Developing Synthetic Methods for Bioactive Phosphorus Compounds Using H-Phosphonate Chemistry. A Progres Report
Nucleos. Nucleot. Nucl. Acids, 24, 353-357  (2005)
T. Johansson, J. Nilsson, M. Kullberg, G. LavŽn, M. Sobkowski, A. Szymanska, M. Szymczak, A. Kraszewski, and J. Stawinski
208. Oxidative Transformations of Nucleoside Fluorenemethyl H-Phosphonoselenoate diesters
Nucleos. Nucleot. Nucl. Acids, 24, 659-661  (2005)
M. Kullberg and J. Stawinski
207. Aryl Nucleoside H-Phosphonates as a Tool for Investigation of Stereospecificity During Coupling
Nucleos. Nucleot.  Nucl. Acids, Accepted 24, 887-890  (2005)
M. Sobkowski, J. Jankowska, J. Stawinski, and A. Kraszewski
206. A Cautionary Note on the Use of the 31P NMR Spectroscopy in Stereochemical Correlation Analysis
Nucleos. Nucleot.  Nucl. Acids, Accepted  24 1033-1046(2005)
M. Sobkowski, J. Jankowska, J. Stawinski, and A. Kraszewski
205. Stereospecific and regioselective opening of an oxirane system. A new efficient entry to 1- or 3-monoacyl- and 1- or 3-monoalkyl-sn-glycerols
Tetrahedron Lett., 46, 1601-1605 (2005)
S. D. Stamatov and J. Stawinski
204. Regioselective Opening of an Oxirane System with Trifluoroacetic Anhydride. A General Method for the Synthesis of 2-Monoacyl- and 1,3-   Symmetrical Triacylglycerols
Tetrahedron, 61, 3659-3669 (2005)
S. D. Stamatov and J. Stawinski
203. Chemical and stereochemical aspects of oxidative coupling of H-phosphonate and H-phosphonothioate diesters.Reactions with N,N-, N,O- and O,O-binucleophiles
Lett. Org. Chem., 2, 188-197 (2005)
J. Nilsson, A. Kraszewski, and J. Stawinski


2001-2004


 


201. Controlling stereochemistry during oxidative coupling. Prparation of Rp and Sp phosphoramidates from on P-chiral precursor.
Chem. Comm, 2566-2567 (2004)
J. Nilsson, and J. Stawinski
201. Silylation-mediated transesterification of phenyl H-phosphonothioates - a new entry to nucleoside H-phosphonothioate monoesters
Eur. J. Org. Chem., 5111-5114 (2004)
G. Laven, J. Nilsson, and J. Stawinski
200. Synthesis of Oligodeoxyribo- and Oligoribonucleotides According to the H-Phosphonate Method
In: Current Protocols in Nucleic Acid Chemistry, ed. S. L. Beaucage, D. E. Bergstrom, G. D. Glick and R. A. Jones, John Wiley & Sons, Inc., New York, p. Chapter 3.4.1 - 3.4.11. Supplement 19 (2004)
R. Strömberg and J. Stawinski
199. Di- and oligonucleotide Synthesis Using H-Phosphonate Chemistry
In: Oligonucleotide Synthesis: Methods and Applications, ed. P. Herdewijn, Humana Press, Totowa, NJ, p. 81-100 (2004)
J. Stawinski and R. Strömberg
198. Dibezyl H-Phosphonate
In: Electronic Encyclopaedia of Reagents for Organic Synthesis [e-EROS], ed. L. A. Paquette, D. Crich, F. Fuchs and P. Wipf, Wiley InterScience
http://www.mrw.interscience.wiley.com/eros/, (2004)
M. Kullberg and J. Stawinski
197. A new approach to stereospecific synthesis of P-chiral phosphorothioates. Preparation of diastereomeric dithymidyl-(3'-5-) phosphorothioates
Chem. Commun.
, 290-291 (2004)
H. Almer, T. Szabo, and J. Stawinski
196. Nucleoside H-phosphonates. Part 19: Efficient entry to novel nucleotide analogues with 2-pyridyl- and 4-pyridylphosphonothioate internucleotide linkages
Tetrahedron
, 60, 389-395 (2004)
T. Johansson and J. Stawinski
195. Aryl nucleoside H-phosphonates. Versatile intermediates in the synthesis of nucleotides and their analogues
Trends in Organic Chemistry,
, 10, 1-19 (2003)
 A. Kraszewski and J. Stawinski
194. H-Phosphonate Chemistry - Advances and Prospects in the Synthesis of Nucleic Acids and Their Analogues
Ann. Pol. Chem. Soc., 2, 119-123 (2003)
J. Stawinski
193. Novel DNA analogues with 2-, 3-, and 4-pyridylphosphonate internucleotide bond: synthesis and hybridization properties
New J. Chem., 27, 1698-1705 (2003)
K. Zmudzka, T. Johansson, M. Wojcik, M. Janicka, M. Nowak, J. Stawinski, and B. Nawrot
192. Aryl H-Phosphonates. Part 14. Synthesis of new Nucleotide Analogues with Phosphonate-Phosphate Internucleosidic Linkage
Org. Lett.
, 5, 3571-3573 (2003)
M. Szymczak, A. Szymanska, J. Stawinski, J. Boryski, and A. Kraszewski
191. Studies Towards Synthesis of Dinucleoside Arylphosphonates with Metal Complexing Properties
Nucleos. Nucleot. Nucl. Acids, 22, 1459-1461 (2003)
T. Johansson and J. Stawinski
190. Developing Synthetic Methods for Bioactive Phosphorus Compounds Using H-Phosphonate Chemistry. A Progress Report
Nucleos. Nucleot. Nucl. Acids, 22, 617-621 (2003)
M. Bollmark, T. Johansson, M. Kullberg, J. Nilsson, J. Stawinski, J. Cieslak, J. Jankowska, M. Sobkowski, M. Szymczak, M. Wenska, and A. Kraszewski
189. Chemoselectivity in Oxidative Coupling of Bifunctional Nucleophiles with Dinucleoside H-Phosphonate and Dinucleoside H-Phosphonothioate Diesters
Nucleos. Nucleot. Nucl. Acids, 22, 1467-1469 (2003)
 J. Nilsson, A. Kraszewski, and J. Stawinski
188. 9-Fluorenemethyl H-Phosphonoselenoate - A Versatile Reagent for Transferring an H-Phosphonoselenoate Group
Nucleos. Nucleot. Nucl. Acids
, 22, 1463-1465 (2003)
M. Kullberg and J. Stawinski
187. Triphenylphosphine Selenide
In: Electronic Encyclopaedia of Reagents for Organic Synthesis [e-EROS], ed. L. A. Paquette, D. Crich, F. Fuchs and P. Wipf, Wiley InterScience  http://www.mrw.interscience.wiley.com/eros/, (2003)
J. Stawinski and M. Bollmark
186. Diphenyl Phosphonate
 In: Electronic Encyclopaedia of Reagents for Organic Synthesis [e-EROS], ed. L. A. Paquette, D. Crich, F. Fuchs and P. Wipf, Wiley InterScience
http://www.mrw.interscience.wiley.com/eros/, (2003)
 J. Stawinski and A. Kraszewski
185. 3H-1,2-Benzothiaselenol-3-one
In: Electronic Encyclopaedia of Reagents for Organic Synthesis [e-EROS], ed. L. A. Paquette, D. Crich, F. Fuchs and P. Wipf, Wiley InterScience
http://www.mrw.interscience.wiley.com/eros/doc/00001/00003328.htm, (2003)
J. Stawinski and M. Thelin
184. H-Pyrophosphonic acid
In: Electronic Encyclopaedia of Reagents for Organic Synthesis [e-EROS], ed. L. A. Paquette, D. Crich, F. Fuchs and P. Wipf, Wiley InterScience
http://www.mrw.interscience.wiley.com/eros/doc/00001/00003329.htm, (2003)
J. Stawinski and M. Thelin
183. How to get the most out of two phosphorus chemistries. Studies on H-phosphonates
Acc. Chem. Res., 35, 952-960 (2002)
 J. Stawinski and A. Kraszewski
182. H-Phosphonates - Chemistry and Applications
 In: Collection Symposium Series, ed. Z. Tocik and M. Hocek, Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague, p. 272-282 (2002)
 J. Stawinski and A. Kraszewski
181. Oxidative coupling of H-phosphonate and H-phosphonothioate diesters. Iodine as a reagent and a catalyst
Collection Symposium Series, 5, 87-92 (2002)
J. Nilsson and J. Stawinski
180. Studies on the synthesis of picolylphosphonate diesters
Collection Symposium Series, 5, 81-86 (2002)
T. Johansson and J. Stawinski
179. Triphenyl phosphoroselenoate - a new selenizing agent for P(III) compounds

Collection Symposium Series, 5, 290-294 (2002)
M. Kullberg, M. Bollmark, and J. Stawinski
178. Dinucleoside aryl phosphorothioates as building blocks for large scale synthesis of chimeric oligonucleotide analogues
Collection Symposium Series, 5, 283-289 (2002)
M. Sobkowski, J. Cieslak, J. Jankowska, J. Stawinski, and A. Kraszewski
177. New synthetic methods for nucleotide analogues based on H-phosphonate chemistry. A progress report
Phosphor. Sulfur Silicon, 177, 1513-1516 (2002)
J. Nilsson, M. Bollmark, J. Jankowska, M. Wenska, J. Cieslak, A. Kraszewski, and J. Stawinski
176. Synthesis of nucleotide analogues with pyridylphosphonate and pyridylphosphonothioate internucleotide linkages
Phosphor. Sulfur Silicon, 177, 1779-1782 (2002)
T. Johansson and J. Stawinski
175. Novel, regioselective transformation of an oxirane system. An efficient approach to the synthesis of endocannabinoid 2-arachidonoylglycerol
Tetrahedron Lett., 43, 1759-1761 (2002)
 S. D. Stamatov and J. Stawinski
174. Aryl H-phosphonates. Part 13. A new, general entry to aryl nucleoside phosphate and aryl nucleoside phosphorothioate diesters
 J. Chem. Soc. Perkin Trans. 1, 31-37 (2002)
 J. Cieslak, J. Jankowska, M. Sobkowski, M. Wenska, J. Stawinski, and A. Kraszewski
173. Nucleoside H-phosphonates. Part 19: Novel nucleotide analogues Ð H-phosphonoselenoate mono- and diesters
Tetrahedron Lett., 43, 515-518 (2002)
M. Bollmark, M. Kullberg, and J. Stawinski
172. Interaction of thymidylate synthase with the 5'-thiophosphates, 5'-dithiophosphates, 5'-H-phosphonates and 5'-S-thiosulfates of 2'-deoxyuridine, thymidine and 5-fluoro-2'-deoxyuridine
Biol. Chem., 382, 1439-1445 (2001)
B. Golos, J. M. Dzik, Z. Kazmierczuk, Z. Zielinski, J. Jankowska, A. Kraszewski, J. Stawinski, W. Rode, and D. Shugar
171. Synthesis of dinucleoside pyridylphosphonates involving palladium(0)-catalysed phosphorus-carbon bond formation as a key step
Chem. Commun., 2564-2565 (2001)
T. Johansson and J. Stawinski
170. Reinvestigation of the 31P NMR evidence for the formation of diorganyl phosphoropyridinium intermediates
J. Chem. Soc. Perkin Trans. 2, 2263-2266 (2001)
J. Nilsson, A. Kraszewski, and J. Stawinski
169. A new method for the synthesis of nucleoside 2,3'-O,O-cyclic phosphorothioates via aryl cyclic phosphites as intermediates
T
etrahedron Lett.
, 42, 8055-8058 (2001)
M. Wenska, J. Jankowska, M. Sobkowski, J. Stawinski, and A. Kraszewsk
168.
Nucleoside phosphate analogues of biological interest and their synthesis via aryl nucleoside H-phosphonates as intermediates
Acta Biochem. Pol., 48, 429-442 (2001)
J. Cieslak, M. Sobkowski, J. Jankowska, M. Wenska, M. Szymczak, B. Imiolczyk, I. Zagorowska, D. Shugar, J. Stawinski, and A. Kraszewski
167.
The  case for configurational stability of H-phosphonate diesters in the presence of diazabicyclo[5.4.0]undec-7-ene (DBU)
Bioorg. Med. Chem., 9, 2315-2322 (2001)
T. Johansson and J. Stawinski
166.
A new selenium-transferring reagent - triphenylphosphine selenide
Chem. Commun., 771-772 (2001)
M. Bollmark and J. Stawinski
165.
Deoxyribo- and Ribonucleoside H-Phosphonates
In: Current Protocols in Nucleic Acid Chemistry, ed. S. L. Beaucage, D. E. Bergstrom, G. D. Glick and R. A. Jones, John Wiley & Sons, Inc., New York, p. Chapter 2.6.1 - 2.6.15 (2001)
J. Stawinski and R. Strömberg
164. 2-Pyridylphosphonates: a new type of modification for nucleotide analogues
Tetrahedron Lett., 42, 2217-2220 (2001)
T. Johansson, A. Kers, and J. Stawinski




1996-2000


1975 - 1980  1986 - 1990 1991 - 1995  1996 - 2000   2001 - 2004   2005 -           



163. Synthetic strategies and parameters involved in the synthesis of oligodeoxyribo- and oligoribonucleotides according to the H-phosphonate method
In: Current Protocols in Nucleic Acid Chemistry, ed. S. L. Beaucage, D. E. Bergstrom, G. D. Glick and R. A. Jones, John Wiley & Sons, Inc., New York, p. Chapter 3.4.1 - 3.4.11 (2000)
R. Strömberg and J. Stawinski
162. A simple and efficient method for direct acylation of acetals with long alkyl-chain carboxylic acid anhydrides
Tetrahedron, 56, 9697-9703 (2000)
S. D. Stamatov and J. Stawinski
161. Aryl H-phosphonates. 12. Synthetic and 31P NMR studies on the preparation of nucleosides H-phosphonothioate and nucleoside H-phosphonodithioate monoesters
J. Org. Chem., 65, 7049-7054 (2000)
J. Cieslak, J. Jankowska, J. Stawinski, and A. Kraszewski
160. Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part VI. Reaction with diols
Nucleoside & Nucleotides, 19, 1487-1503 (2000)
M. Sobkowski, M. Wenska, A. Kraszewski, and J. Stawinski
159. A new, efficient entry to nucleoside 2',3'-O,O-cyclophosphorothioates
Tetrahedron Lett., 41, 2227-2229 (2000)
J. Jankowska, M. Wenska, M. Popenda, J. Stawinski, and A. Kraszewski
158. Aryl H-phosphonates. Part 11. Synthetic and 31P NMR studies on the formation of aryl nucleoside H-phosphonates
J. Chem. Soc. Perkin Trans. 1, 3327-3331 (1999)
J. Cieslak, M. Szymczak, M. Wenska, J. Stawinski, and A. Kraszewski
157. Synthesis and anti-retroviral activity of O,O-bis(3'-azido-2',3'-dideoxythymidin-5'-yl) phosphoramidate derivatives
Nucleosides & Nucleotides, 18, 2317-2325 (1999)
I. Kers, J. Stawinski, J.-L. Girardet, J.-L. Imbach, C. Perigaud, G. Gosselin, and A.-M. Aubertin
156. New methods for the formation of the P-N and P-F bonds, their relevance to nucleotide and oligonucleotide  analogues synthesis
Phosphor. Sulfur Silicon, 144-146, 637-640 (1999)
I. Kers, M. Bollmark, A. Kraszewski, and J. Stawinski
155. Studies on enzymatic hydrolysis of thymidin-3'-yl thymidin-5'-yl phosphorofluoridates and the corresponding phosphorothiofluoridates
Chem. Commun., 2115-2116 (1999)
K. Misiura, M. Bollmark, J. Stawinski, and W. J. Stec
154. Studies on the reaction of trityl derivatives with H-phosphonate diesters: Their relevance to the synthesis of 4-pyridylphosphonates
Heteroatom Chem., 10, 492-499 (1999)
A. Kers, L. Dembkowski, A. Kraszewski, and J. Stawinski
153. The reaction of diphenyl and dialkyl phosphorochloridates with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Formation of phosphonate diesters via N->C phosphorus migration
J. Chem. Soc. Perkin Trans. 2, 2071-2075 (1999)
A. Kers, I. Kers, and J. Stawinski
152. Preparation of nucleoside 5 '-deoxy-5 '-methylenephosphonates as building blocks for the synthesis of methylenephosphonate analogues
J. Chem. Soc. Perkin Trans. 1, 2585-2590 (1999)
A. Kers, T. SzabÑ, and J. Stawinski
151. Aryl H-Phosphonates. 10. Synthesis of nucleosides phosphoramidate and nucleoside phosphoramidothioate analogues via H-phosphonamidate intermediates
Tetrahedron, 55, 11579-11588 (1999)
A. Kers, J. Stawinski, and A. Kraszewski
150. Developing synthetic methods for nucleotide analogues. A progress report
In: Collection Symposium Series, ed. A. Holy and M. Hocek, Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague, p. 69-74 (1999)
A. Kers, I. Kers, J. Stawinski, J. Cieslak, J. Jankowska, and A. Kraszewski
149. The reactions of aryl nucleoside H-phosphonates with O-, N-, and S-nucleophiles
In: Collection Symposium Series, ed. A. Holy and M. Hocek, Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague, p. 63-68 (1999)
J. Cieslak, J. Jankowska, M. Sobkowski, A. Kers, I. Kers, J. Stawinski, and A. Kraszewski
148. Studies on sulfurisation of H-phosphonate diesters in the presence of diazabicyclo[5.4.0]unde-7-ene (DBU)
Collection Symposium Series, 2, 75-78 (1999)
T. Johansson, M. Bollmark, and J. Stawinski
147. A New Type of Nucleotide Analogue with 4-Pyridylphosphonate Internucleotide Linkage
Tetrahedron Lett., 40, 4263-4266 (1999)
A. Kers and J. Stawinski
146. A mild method for the preparation of nucleoside phosphorofluoridate and phosphorofluoridothioate diesters
Nucleosides & Nucleotides, 18, 1243-1244 (1999)
M. Bollmark and J. Stawinski
145. Aryl H-Phosphonates. 8. Simple and Efficient Method for the Preparation of Nucleoside H-Phosphonothioate Monoesters
Tetrahedron Lett., 40, 3945-3948 (1999)
I. Kers, A. Kers, J. Stawinski, and A. Kraszewski
144. Synthesis and in vitro evaluation of antiviral activity of some symmetrical phosphoramidate triesters of AZT
Nucleosides & Nucleotides, 18, 993-994 (1999)
I. Kers, J.-L. Girardet, G. Gosselin, C. Perigaud, J.-L. Imbach, and J. Stawinski
143. Aryl nucleoside H-phosphonates - novel derivatives of controlled reactivity
Nucleosides & Nucleotides, 18, 937-938 (1999)
J. Cieslak, J. Jankowska, M. Szymczak, A. Kers, I. Kers, J. Stawinski, and A. Kraszewski
142. New methods for multiple modifications of a phosphorus center
Nucleosides & Nucleotides, 18, 1245-1246 (1999)
M. Bollmark, J. Cieslak, J. Jankowska, I. Kers, A. Kraszewski, and J. Stawinski
141. 31P NMR studies on oxidative transformation of aryl nucleoside H-phosphonate diesters
Nucleosides & Nucleotides, 18, 991-992 (1999)
A. Kers, I. Kers, A. Kraszewski, and J. Stawinski
140. Reaction of H-phosphonate diesters with trityl halides
Phosphorus, Sulfur, Silicon, 147, 167 (1999)
A. Kers and J. Stawinski
139. Nucleoside phosphoramidate analogues with modification in the bridging position of the phosphodiester linkage
Phosphorus, Sulfur, Silicon, 147, 169 (1999)
I. Kers, A. Kraszewski, and J. Stawinski
138. H-Phosphonate chemistry in the synthesis of nucleotides and their analogues
In: Nucleic Acids and Their Constituents. Chemical Evolution Underlying Biological Evolution, ed. A. Wojtowicz, Scientific Publishers OWN, Poznan, p. 16 (1998)
J. Stawinski
137. Some aspects of oligoribonucleotides synthesis via the H-phosphonate approach
Acta Biochem. Pol., 45, 907-915 (1998)
J. Stawinski and A. Kraszewski
136. Hydration of CH3 groups in natural dithymidine nucleotide and its methylphosphonate analogues
Acta Biochem. Pol., 45, 977-985 (1998)
K. Kulinska, T. Kulinski, and J. Stawinski
135. A cautionary note on the use of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in conjunction with chlorophosphates Acta Chem. Scand., 52, 1405-1406 (1998)
A. Kers, I. Kers, M. Bollmark, and J. Stawinski
134. Nucleoside H-Phosphonates. 18. Synthesis of Unprotected Nucleoside 5'-H-Phosphonates and Nucleoside 5'-H-phosphonothioates and their Conversion into the 5'-Phosphorothioate and 5'-Phosphorodithioate Monoesters
J. Org. Chem., 63, 8150-8156 (1998)
J. Jankowska, A. Sobkowska, J. Cieslak, M. Sobkowski, A. Kraszewski, J. Stawinski, and D. Shugar
133. The reactions of H-phosphonates with bifunctional reagents. Part V. Functionalization of support-bound oligonucleotides and synthesis of non-radioactive hybridization probes
 Nucleosides Nucleotides, 17, 253-267 (1998)
M. Sobkowski, A. Kraszewski, and J. Stawinski
132. Nucleotide analogues containing the P-F bond. An overview of the synthetic methods
Nucleosides & Nucleotides, 17, 663-680 (1998)
M. Bollmark and J. Stawinski
131. Molecular dynamics computer simulation study of nucleotide analogues. Comparison of the hydration pattern of dithymidine phosphate with those of dithymidine methylphosphonate diastereomers
J. Biomol. Struct. Dynam., 15, 987-998 (1998)
K. Kulinska, T. Kulinski, J. Stawinski, and A. Laaksonen
130. A new synthetic method for the preparation of nucleoside phosphoramidate analogues with the nitrogen atom in bridging positions of the phosphoramidate linkage
Tetrahedron Lett.
, 39, 1219-1222 (1998)
I. Kers, J. Stawinski, and A. Kraszewski
129. Interaction of thymidylate synthase with the 5'-thiophosphates and 5'-H-phosphonates of 2'-deoxyuridine, thymidine and 5-fluoro-2'-deoxyuridine
In: Chemistry and Biology of Pteridines and Folates, ed. W. Pfleiderer and H. Rokos, Blackwell Science, Berlin, p. 423-426 (1997)
B. Golos, J. M. Dzik, W. Rode, J. Jankowska, A. Kraszewski, J. Stawinski, and D. Shugar
128. Studies on nucleoside phosphonates and their derivatives. A progress report
Nucleosides Nucleotides, 16, 679-684 (1997)
M. Bollmark, A. Kers, I. Kers, T. SzabÑ, R. Zain, J. Stawinski, J. Cieslak, J. Jankowska, and A. Kraszewski
127. Aryl H-phosphonates. 7. Studies on the formation of phosphorus-carbon bond in the reaction of trityl and benzyl halides with dialkyl and diphenyl H-phosphonates
Tetrahedron, 53, 12691-12698 (1997)
A. Kers, J. Stawinski, L. Dembkowski, and A. Kraszewski
126. FTIR Study on nucleotide analogues. 1. Spectral characterization of dinucleoside methylphosphonates and dinucleoside 5'-methylenephosphonates in solution and in solid phase
J. Biomol. Struct. Dynam., 15, 119-128 (1997)
K. Kulinska, J. Sarzynska, T. SzabÑ, and J. Stawinski
125. Aryl H-Phosphonates. Part 6. Synthetic studies on the preparation of nucleosides N-Alkyl-H-Phosphonamidates
J. Org. Chem., 62, 4791-4794 (1997)
A. Sobkowska, M. Sobkowski, J. Cieslak, A. Kraszewski, I. Kers, and J. Stawinski
124. A new method for the formation of the P-F bond
Chem. Commun., 991-992 (1997)
M. Bollmark and J. Stawinski
123. 9-Fluorenemethyl H-phosphonothioate, a versatile reagent for the preparation of H-phosphonothioate, phosphorothioate, and phosphorodithioate monoesters
Tetrahedron Lett., 38, 2007-2010 (1997)
J. Jankowska, J. Cieslak, A. Kraszewski, and J. Stawinski
122. Studies on nucleoside H-phosphonothioates as synthons in the synthesis of oligonucleotide analogues
Nucleosides & Nucleotides, 16, 1661-1662 (1997)
R. Zain, M. Bollmark, and J. Stawinski
121. 31P NMR studies on the activation pathways of aryl H-phosphonate esters with condensing agents
Coll. Czech. Chem. Commun. (Special Issue), 61, S246-249 (1996)
A. Kers, I. Kers, A. Kraszewski, and J. Stawinski
120. Aryl H-phosphonates. Part IV. A new method for internucleotide bond formation based on transesterification of aryl nucleoside H-phosphonate diesters
Tetrahedron Lett., 37, 4561-4564 (1996)
J. Cieslak, M. Sobkowski, A. Kraszewski, and J. Stawinski
119. Solid support synthesis of all Rp-oligoribonucleoside phosphorothioates
Nucleic Acids Res., 24, 3811-3820 (1996)
H. Almer, J. Stawinski, and R. Stršmberg
118. Nucleoside H-phosphonates. 17. Synthetic and 31P NMR studies on the preparation of dinucleoside H-phosphonothioates
J. Org. Chem., 61, 6617-6622 (1996)
R. Zain and J. Stawinski
117. A facile access to nucleoside phosphorofluoridate, nucleoside phosphorofluoridothioate, and nucleoside phosphorofluoridodithioate monoesters
Tetrahedron Lett., 37, 5739-5742 (1996)
M. Bollmark and J. Stawinski
116. Studies on aryl H-phosphonates. 3. Mechanistic investigations related to the disproportionation of diphenyl H-phosphonate under anhydrous basic conditions
Tetrahedron, 52, 9931-9944 (1996)
 A. Kers, I. Kers, J. Stawinski, M. Sobkowski, and A. Kraszewski
115. Efficient method for the preparation of nucleoside phosphorofluoridates and nucleoside phosphorofluoridothioates
Coll. Czech. Chem. Commun. (Special Issue), 61, S68-71 (1996)
M. Bollmark, R. Zain, and J. Stawinski
114. Synthetic applications of aryl H-phosphonates in nucleotide chemistry
Coll. Czech. Chem. Commun. (Special Issue), 61, S242-245 (1996)
J. Cieslak, J. Jankowska, A. Sobkowska, M. Sobkowski, A. Kraszewski, A. Kers, I. Kers, and J. Stawinski
113. Aryl H-phosphonates. Part 5. A simple method for the synthesis of aminoalkyl H-phosphonate monoesters via transesterification of diphenyl H-phosphonate with amino alcohols
Coll. Czech. Chem. Commun. (Special Issue), 61, S238-241 (1996)
M. Sobkowski, J. Stawinski, and A. Kraszewski
112. A new entry to nucleoside phosphorofluoridate and nucleoside phosphorofluoridothioate diesters
Tetrahedron Lett., 37, 3537-3540 (1996)
M. Bollmark, R. Zain, and J. Stawinski
111. Exploring reactions of nucleoside H-phosphonates with bifunctional reagents
Phosphor. Sulfur Silicon, 109-110, 261-264 (1996)
J. Stawinski, A. Kraszewski, and M. Sobkowski
110. Nucleoside phosphonates. Development of synthetic methods and reagents
Nucleosides Nucleotides, 15, 361-378 (1996)
A. Kers, I. Kers, A. Kraszewski, M. Sobkowski, T. SzabÑ, M. Thelin, R. Zain, and J. Stawinsk
109. Nucleoside H-phosphonates. 16. 31P NMR studies on the transformation of nucleoside H-phosphonate monoesters into a monofunctional tervalent intermediate, nucleoside acyl silyl phosphites
J. Chem. Soc. Perkin Trans. 2, 795-799 (1996)
R. Zain and J. Stawinski


 

1991-1995


1975 - 1980  1986 - 1990 1991 - 1995  1996 - 2000   2001 - 2004   2005 -       

 


108. Nucleoside H-phosphonates. 15. Preparation of nucleoside H-phosphonothioate monoesters from the corresponding nucleoside H-phosphonates
J. Org. Chem., 60, 8241-8244 (1995)
R. Zain, R. Stršmberg, and J. Stawinski
107. A new approach to the synthesis of the 5'-deoxy-5'-methylphosphonate linked thymidine oligonucleotide analogues
Nucleic Acids Res., 23, 893-900 (1995)
T. Szabo, A. Kers, and J. Stawinski
106. RNA-Synthesis using the H-phosphonate approach and an improved protecting group strategy
Nucleosides Nucleotides, 14, 883-887 (1995)
E. Westman, S. Sigurdsson, H. Almer, M. Thelin, J. Stawinski, E. Rozners, and R. Strömberg
105. Solid phase synthesis of 5'-methylenephosphonate DNA
Nucleosides Nucleotides, 14, 871-874 (1995)
T. Szabo, A. Kers, and J. Stawinski
104. 2-Cyanoethyl H-phosphonate. A reagent for the mild preparation of nucleoside H-phosphonate monoesters
Nucleosides Nucleotides, 14, 715-716 (1995)
T. Szabo, H. Almer, R. Strömberg, and J. Stawinski
103. Conversion of nucleoside H-phosphonate monoesters to the corresponding H-phosphonothioates. 31P NMR studies
Nucleosides & Nucleotides, 14, 711-714 (1995)
J. Stawinski and R. Zain
102. Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part 3. Further studies on transesterification of nucleoside H-phosphonate diesters with amino alcohols
Nucleosides Nucleotides, 14, 839-842 (1995)
M. Sobkowski, J. Stawinski, A. Sobkowska, and A. Kraszewski
101. Studies on aryl H-phosphonates. Synthesis of nucleoside N-alkylphosphonamidates
Nucleosides Nucleotides, 14, 703-706 (1995)
A. Sobkowska, M. Sobkowski, J. Stawinski, and A. Kraszewski
100. Chemical synthesis of RNA-fragment analogues that have phosphorothioate linkages of identical configuration
Nucleosides Nucleotides, 14, 879-881 (1995)
H. Almer, J. Stawinski, and R. Strömberg
99. Synthesis and some conformational features of the 5'-deoxy-5'-methylphosphonate linked dimer, 5'-deoxy-5-C-(phosphonomethyl)thymidin-3'-yl (thymidin-5'-yl)methylphosphonate [pCH2)Tp(CH2)T]
Tetrahedron, 51, 4145-4160 (1995)
T. Szabo and J. Stawinski
98. The SP diastereomer of a dinucleoside methylphosphonate methanol solvate containing thymine and N3-methyl-4-thiothymine bases
Acta Cryst., C51, 411-415 (1995)
T. Szabo, J. Stawinski, S. Carlson, and R. Norrestam
97. Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part 4. Chemoselectivity during oxidative coupling of nucleoside H-phosphonate diesters with amino alcohols controlled by protonation of the amino function
Tetrahedron Lett., 36, 2295-2298 (1995)
M. Sobkowski, J. Stawinski, and A. Kraszewski
96. Studies on aryl H-phosphonates. Part 2. A general method for the preparation of alkyl H-phosphonate monoesters
Synthesis, 427-430 (1995)
 A. Kers, I. Kers, J. Stawinski, M. Sobkowski, and A. Kraszewski
95.
RNA synthesis using H-phosphonates
Am. Chem. Soc. Meeting, 207, 83Cab (1994)
P. J. Garegg, J. Stawinski, R. Stršmberg, and E. Westman
94. Improving the H-phosphonate approach to oligoribonucleotide synthesis
Nucleic Acids Sym. Ser., 31, 25 (1994)
E. Westman, S. Sigurdsson, J. Stawinski, and R. Strömberg
93. Photochemistry of di(deoxyribonucleoside) methylphosphonates containing N3-methyl-4-thiothymine
J. Org. Chem., 59, 7273-7283 (1994)
P. Clivio, J.-L. Fourrey, T. SzabÑ, and J. Stawinski
92. Synthesis of stereochemically homogeneous oligoribonucleoside all-Rp-phosphorothioates by combining H-phosphonate chemistry and enzymatic digestion
J. Chem. Soc. Chem. Commun., 1459-1460 (1994)
H. Almer, J. Stawinski, and R. Strömberg
91. Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part 2. Stability of nucleoside H-phosphonate diesters in the presence of amino alcohols
J. Chem. Soc. Perkin Trans. 1, 1803-1808 (1994)
M. Sobkowski, J. Stawinski, A. Sobkowska, and A. Kraszewski
90. Studies on aryl H-phosphonates. I. Efficient method for the preparation of deoxyribo- and ribonucleoside 3'-H-phosphonate monoesters by transesterification of diphenyl H-phosphonate
Tetrahedron Lett., 35, 3355-3358 (1994)
J. Jankowska, M. Sobkowski, J. Stawinski, and A. Kraszewski
89. Nucleoside H-Phosphonates. 14. Synthesis of Nucleoside Phosphoroselenoates and Phosphorothioselenoates via Stereospecific Selenization of the Corresponding H-Phosphonate and H-Phosphonothioate Diesters with the Aid of New Selenium-Transfer Reagent 3H-1,2-Benzothiaselenol-3-one
J. Org. Chem., 59, 130-136 (1994)
J. Stawinski and M. Thelin
88.
Hydrolytic stability of nucleoside H-phosphonate and H-phosphonothioate diesters
Collect. Czech. Chem. Commun. (Special issue), 58, 79-81 (1993)
J. Stawinski, R. Strömberg, and R. Zain
87. RNA-Synthesis using H-phosphonates. Synchronizing 2'-OH and N-protection
Collect. Czech. Chem. Commun. (Special Issue), 58, 236-237 (1993)
E. Westman, J. Stawinski, and R. Strömberg
86.
Molecular and crystal structure of Sp-thymidin-3'-yl 4-thiothymidin-5'-yl methylphosphonate
Nucleic Acids Res., 21, 3921-3926 (1993)
T. Szabo, D. Noreus, R. Norrestam, and J. Stawinski
85.
5'-Hydrogenphosphonates of anti-HIV nucleoside analogues revisited: controversial mode of action
Antiviral Res., 22, 143-153 (1993)
G. Gosselin, C. PŽrigaud, I. Lefebvre, A. Pompon, A.-M. Aubertin, A. Kirn, T. Szabo, J. Stawinski, and J.-L. Imbach
84. Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part 1. Reaction with amino alcohols
J. Chem. Soc. Perkin Trans. I, 1699-1704 (1993)
A. Kraszewski, M. Sobkowski, and J. Stawinski
83.
H-Phosphonates in Oligonucleotide Synthesis
Trends Org. Chem., 4, 31-67 (1993)
J. Stawinski and R. Strömberg
82.
3H-1,2-Benzothiaselenol-3-one. A new selenizing reagent for nucleoside H-phosphonate and H-phosphonothioate diesters
Tetrahedron Lett., 33, 7255-7258 (1992)
J. Stawinski and M. Thelin
81. Synthesis of diribonucleoside phosphorothioates via stereospecific sulfurization of H-phosphonate diesters
J. Org. Chem., 57, 6163-6169 (1992)
H. Almer, J. Stawinski, R. Strömberg, and M. Thelin
80. Some Aspects of H-Phosphonate Chemistry
In: Handbook of Organophosphorus Chemistry, ed. R. Engel, Marcel Dekker, New York, p. 377-434 (1992)
J. Stawinski
79. Stereospecific oxidation and oxidative coupling of H-phosphonate and H-phosphonothioate diesters
Tetrahedron Lett., 33, 3185-3188 (1992)
J. Stawinski, R. Stršmberg, and R. Zain
78.
3H-2,1-Benzoxathiol-3-one 1-oxide. A new reagent for stereospecific oxidation of nucleoside H-phosphonothioate diesters
Tetrahedron Lett., 33, 3189-3192 (1992)
J. Stawinski and M. Thelin
77.
Synthesis and Chemical-Properties of Some Thio Analogs of Nucleoside H-Phosphonates
Am. Chem. Soc. Meeting, 201, 10-CARB (1991)
J. Stawinski, R. Strömberg, T. Szabo, M. Thelin, E. Westman, and R. Zain
76. Some chemical and stereochemical aspects of ribonucleoside H-phosphonate and H-phosphonothioates diester synthesis
Nucleosides & Nucleotides, 10, 511-514 (1991)
J. Stawinski, R. Strömberg, and M. Thelin
75. Studies on the conversion of nucleoside H-phosphonate monoesters into the corresponding H-phosphonothioates
Nucleosides & Nucleotides, 10, 515-516 (1991)
J. Stawinski, R. Strömberg, and R. Zain
74.
Studies on sulfurization of nucleoside H-phosphonate and H-phosphonothioate esters using 3H-1,2-benzodithiol-3-one 1,1-dioxide
Nucleosides Nucleotides, 10, 517-518 (1991)
J. Stawinski, M. Thelin, and E. von Stedingk
73.
Ribonucleoside H-phosphonates. Pyridine vs quinoline - influence on condensation rate
Nucleosides Nucleotides, 10, 519-520 (1991)
J. Stawinski, R. Strömberg, and E. Westman
72. Nucleoside H-Phosphonates. 13. Studies on 3H-1,2-benzodithiol-3-one derivatives as sulfurizing reagents for H-phosphonate and H-phosphonothioate diesters
J. Org. Chem., 56, 5169-5175 (1991)
J. Stawinski and M. Thelin
71. Studies directed towards efficient synthesis of oligo-5'-deoxy-5-C-(phosphonomethyl)deoxyribonucleosides
Nucleic Acids Sym. Ser., 24, 71-72 (1991)
J. Stawinski and T. Szabo
70.
Synthesis and some reactions of nucleoside H-phosphonothioate esters
Nucleic Acids Sym. Ser., 24, 95-98 (1991)
J. Stawinski, R. Strömberg, T. Szabo, M. Thelin, E. Westman, and R. Zain
69. Synthesis of diribonucleoside thiophosphates via stereospecific sulfurization of H-phosphonates
Nucleic Acids Sym. Ser., 24, 227 (1991)
H. Almer, J. Stawinski, R. Strömberg, and M. Thelin
68. Studies on reaction conditions for ribonucleotide synthesis via the H-phosphonate approach
Nucleic Acids Sym. Ser., 24, 228 (1991)
J. Stawinski, R. Strömberg, and E. Westman
67. Convenient synthesis of dinucleotide methylphosphonates
Nucleic Acids Sym. Ser., 24, 229 (1991)
J. Stawinski, R. Strömberg, and T. Szabo
66.
Some chemical and stereochemical aspects of oxidation of nucleoside H-phosphonothioate diesters
Nucleic Acids Sym. Ser., 24, 230 (1991)
J. Stawinski, R. Strömberg, and R. Zain
 
 

 

  1986-1990

1975 - 1980  1986 - 1990 1991 - 1995  1996 - 2000   2001 - 2004   2005 -         

 



65. Studies on the activation pathway of phosphonic acid using acyl chlorides as activators
J. Chem. Soc. Perkin Trans. II, 849-853 (1990) 
J. Stawinski and M. Thelin
64. Nucleoside H-Phosphonates. XI. A Convenient Method for the Preparation of Nucleoside H-Phosphonates
Nucleosides Nucleotides, 9, 129-135 (1990)
J. Stawinski and M. Thelin
63. Studies on the preparation of nucleoside H-phosphonothioates
Collect. Czech. Chem. Commun., 55, 141-144 (1990)
J. Stawinski, T. Szabo, M. Thelin, E. Westman, and R. Zain
62. Synthesis of nucleoside methylphosphonates and nucleoside methylphosphonothioates via phosphinate intermediates
Collect. Czech. Chem. Commun., 55, 145-148 (1990)
J. Stawinski, R. Strömberg, and T. SzabÑ
61. Nucleoside H-Phosphonates. XII. Synthesis of Nucleoside 3'-Hydrogenphosphonothioate Monoesters via Phosphinate Intermediates
J. Org. Chem., 55, 3503-3506 (1990)
J. Stawinski, M. Thelin, E. Westman, and R. Zain
60. Nucleoside H-Phosphonates. X. Studies on Nucleoside Hydrogenphosphonothioate Diester Synthesis
Tetrahedron Lett., 30, 2157-2160 (1989)
J. Stawinski, M. Thelin, and R. Zain
59.
A general method for the synthesis of glycerophospholipids and their analogues via H-phosphonate intermediates
J. Org. Chem., 54, 1338-1342 (1989)
I. Lindh and J. Stawinski
58. Recent studies in nucleoside phosphonate chemistry
Nucleosides Nucleotides, 8, 1029-1032 (1989)
J. Stawinski, R. Strömberg, T. Szabo, and E. Westman
57. The H-phosphonate method for constructing phosphodiester linkages. A progress report
Nucleosides Nucleotides, 8, 799-803 (1989)
J. Stawinski, R. Strömberg, I. Lindh, T. Regberg, T. Szabo, M. Thelin, E. Westman, and P. J. Garegg
56. Recent Studies on Nucleoside H-Phosphonothioates and Nucleoside Methylphosphonothioates Synthesis
Nucleic Acids Sym. Ser., 21, 47-48 (1989)
J. Stawinski, T. Szabo, M. Thelin, E. Westman, and R. Zain
55. Nucleoside H-Phosphonates. IX. Possible Side-Reactions during Hydrogenphosphonate Diester Formation
Nucleosides Nucleotides, 7, 23-35 (1988)
T. Regberg, J. Stawinski, and R. Strömberg
54.
Studies on the t-butyldimethylsilyl group as 2'-O-protection in oligoribonucleotide synthesis via the H-phosphonate approach
Nucleic Acids Res., 16, 9285-9298 (1988)
J. Stawinski, R. Strömberg, M. Thelin, and E. Westman
53. Evaluation of the use of the t-butyldimethylsilyl group for 2Ç-protection in RNA synthesis via the H-phosphonate approach
Nucleosides Nucleotides, 7, 779-782 (1988)
J. Stawinski, R. Strömberg, M. Thelin, and E. Westman
52. Reactions of nucleoside hydrogenphosphonates with diphenylchlorophosphate and sterically hindered aromatic acyl chlorides
Nucleosides Nucleotides, 7, 601-604 (1988)
J. Stawinski, R. Strömberg, M. Thelin, and E. Westman
51. Studies on Ribonucleoside Hydrogenphosphonates. Effect of a Vicinal Hydroxy Function on the Stability of H-Phosphonate Diester Bond
Nucleosides Nucleotides, 7, 321-337 (1988)
S. Huss, G. Gosselin, J. Stawinski, R. Strömberg, and J.-L. Imbach
50.
Nucleoside H-Phosphonates. VIII. Activation of Hydrogenphosphonate Monoesters by Chlorophosphates and Aryl Sulfonyl Derivatives
J. Org. Chem., 52, 284-287 (1987)
P. J. Garegg, J. Stawinski, and R. Strömberg
49. Nucleoside H-Phosphonates. VI. Reaction of Nucleoside Hydrogenphosphonates with Arenesulfonyl Chlorides
J. Chem. Soc. Perkin Trans. II, 1209-1214 (1987)
P. J. Garegg, J. Stawinski, and R. Strömberg
48.
Nucleoside H-Phosphonates. VII. Studies on the Oxidation of Nucleoside Hydrogenphosphonate Esters
J. Chem. Soc. Perkin Trans. I, 1269-1273 (1987)
P. J. Garegg, T. Regberg, J. Stawinski, and R. Strömberg
47. Studies on the Oxidation of Nucleoside Hydrogenphosphonates
Nucleosides Nucleotides, 6, 429-432 (1987)
P. J. Garegg, T. Regberg, J. Stawinski, and R. Strömberg
46. Activation of Nucleoside Hydrogenphosphonates by Use of Aryl Sulfonyl Chlorides
Nucleosides Nucleotides, 6, 425-427 (1987)
P. J. Garegg, J. Stawinski, and R. Strömberg
45. Studies on the synthesis of oligonucleotides via the hydrogenphosphonate approach
Nucleosides Nucleotides, 6, 283-286 (1987)
P. J. Garegg, T. Regberg, J. Stawinski, and R. Strömberg
44. Evaluation of Some New Condensing Reagents for Hydrogenphosphonate Diester Formation
Nucleic Acids Sym. Ser., 18, 185-188 (1987)
R. Strömberg and J. Stawinski
43. Synthesis of Phospholipids and Nucleoside-Phospholipids Conjugates via Hydrogenphosphonate Intermediates
Nucleic Acids Sym. Ser., 18, 189-192 (1987)
I. Lindh and J. Stawinski
42. Nucleosides H-Phosphonates. V. The Mechanism of Hydrogenphosphonate Diester Formation Using Acyl Chlorides as Coupling Agents in Oligonucleotide Synthesis by the Hydrogenphosphonate Approach
Nucleosides Nucleotides
, 6, 655-662 (1987)
P. J. Garegg, T. Regberg, J. Stawinski, and R. Strömberg
41. A Phosphorus NMR Studies on the Conversion of Hydroxy-Group into Iodo-Group in Carbohydrates Using the Iodine-Triphenylphosphine-Imidazole Reagent
J. Chem. Soc. Perkin Trans. II, 271-274 (1987)
P. J. Garegg, T. Regberg, J. Stawinski, and R. Strömberg
40. Iodide and Iodine Catalysed Phosphorylation of Nucleosides by Phosphorodiester Derivatives
Nucleosides Nucleotides, 6, 815-820 (1987)
R. Strömberg and J. Stawinski
39. Synthesis of Trinucleoside Monophosphates Using Nucleoside H-Phosphonates
In: Biophosphates and Their Analogues - Synthesis, Structure, Metabolism and Activity, ed. K. S. Bruzik and W. J. Stec, Elsevier, Amsterdam, p. 89-92 (1987)
P. J. Garegg, I. Lindh, and J. Stawinski
38. Automated Solid Phase Synthesis of DNA and RNA Fragments by the Hydrogenphosphonate Approach
In: Biophosphates and Their Analogues - Synthesis, Structure, Metabolism and Activity, ed. K. S. Bruzik and W. J. Stec, Elsevier, Amsterdam, p. 93-98 (1987)
P. J. Garegg, C. Henrichson, I. Lindh, T. Regberg, J. Stawinski, and R. Strömber
37. Influence of the cationic part of nucleoside phosphorodiester on the rate of condensation during oligonucleotide synthesis
In: Biophosphates and Their Analogues - Synthesis, Structure, Metabolism and Activity, ed. K. S. Bruzik and W. J. Stec, Elsevier, Amsterdam, p. 83-87 (1987)
B. Hernes, H. Sobkowska, A. Kraszewski, and J. Stawinski
36. The Role of Tetrazole in Oligonucleotide Synthesis via Phosphotriester Approach
Chem. Scr., 26, 63-65 (1986)
P. J. Garegg, T. Regberg, J. Stawinski, and R. Stršmberg
35. A Further Example of Chemical Synthesis and Cloning of Human Insulin Genes
Chem. Scr., 26, 97-101 (1986)
A. Kraszewski, J. Stawinski, J. Jankowska, B. Stuczynska, and M. Wiewiorowski
34. Studies on the Reaction of Nucleoside Phosphorodiesters with Aryl Sulfonyl Chlorides
Tetrahedron Lett., 27, 2665-2666 (1986)
P. J. Garegg, T. Regberg, J. Stawinski, and R. Stršmberg
33. Nucleoside Hydrogenphosphonates in Oligonucleotide Synthesis
Chem. Scr., 26, 59-62 (1986)
P. J. Garegg, T. Regberg, J. Stawinski, and R. Stršmberg
32. Nucleoside H-Phosphonates. III. Chemical Synthesis of Oligodeoxyribonucleotides by the Hydrogenphosphonate Approach
Tetrahedron Lett., 27, 4051-4054 (1986)
P. J. Garegg, I. Lindh, T. Regberg, J. Stawinski, R. Stršmberg, and C. Henrichson
31. Nucleoside H-Phosphonates. IV. Automated Solid Phase Synthesis of Oligoribonucleotides by the Hydrogenphosphonate Approach
Tetrahedron Lett., 27, 4055-4058 (1986)
P. J. Garegg, I. Lindh, T. Regberg, J. Stawinski, R. Strömberg, and C. Henrichson

  

 

1981-1985



1975 - 1980  1986 - 1990 1991 - 1995  1996 - 2000   2001 - 2004   2005 -         

 



30. Formation of Internucleotidic Bond via Phosphonate Intermediates
Chem. Scr., 25, 280-282 (1985)
P. J. Garegg, T. Regberg, J. Stawinski, and R. Stršmberg
29. Polski projekt biosyntezy insuliny czlowieka
Wiadomosci Chem., 39, 269-270 (1984)
A. Kraszewski and J. Stawinski
28. A Facile Synthesis of Cyclic Phosphorodiesters
Synthesis, 5, 408-410 (1984)
J. Jankowska and J. Stawinski
27. Studies on the influence of tetrazole and N-methylimidazole on the rate of condensation using arylsulfonyl azolides
Nucleic Acids Sym. Ser., 14, 297-298 (1984)
H. Sobkowska, B. Hernes, A. Kraszewski, and J. Stawinski
26. The human preproinsulin gene: synthesis, cloning, gene modification and expression studies
Can. J. Biochemistry Cell Biol., 62, 209-216 (1984)
S. A. Narang, R. Brousseau, F. Georges, J. Michniewicz, G. Prefontaine, J. Stawinski, and W. Sung
25. Synthesis of human insulin gen. VII. Synthesis of preproinsulin-like human DNA, its cloning and expression in M13 bacteriophage
Gene, 27, 201-211 (1984)
P. Georges, R. Brousseau, J. Michniewicz, J. Prefontaine, J. Stawinski, W. Sung, R. Wu, and S. A. Narang
24. Technology of DNA Recombination - Genetic Engineering
Wiadomosci Chem., 39, 129-144 (1984)
J. Stawinski and A. Wolanski
23. Total synthesis and expression of human preproinsulin gene
Genetics - New Frontiers, Proc. 15th Inter. Congr. 1983, 2, 81-90 (1984)
S. A. Narang, R. Brousseau, F. Georges, Z. Hanna, J. Michniewicz, G. Prefontaine, J. Stawinski, J. Stepien, and W. Sung
22. Chemical Synthesis of 5'-Phosphorylated DNA Fragments and Their Constituents
Bull. Acad. Pol. Sci. ser. chim., 31, 17-22 (1983)
J. Jankowska and J. Stawinski
21. Application of Synthetic DNA Fragments in Molecular Biology
Postepy Biochemii, 1-2, 45-69 (1982)
J. Stawinski
20. Studies on the new phosphate protective groups
Nucleic Acids Sym. Ser., 9, 135-139 (1981)
A. Kraszewski and J. Stawinski
19 p-Anisoyltetrazole - a New Anizoylating Reagent
Bull. Acad. Pol. Sci. ser. chim., 29, 483-487 (1981)
J. Stawinski, K. Grzeskowiak, and A. Kraszews


 




18 Further studies on oligoribonucleotide synthesis
Nucleic Acids Sym. Ser., 7, 115-127 (1980)
R. W. Adamiak, E. Biala, K. Grzeskowiak, R. Kierzek, A. Kraszewski, W. T. Markiewicz, J. Stawinski, and M. Wiewiorowski
17. Phosphoryl Tris-Triazole - a New Phosphorylating Reagent
Tetrahedron Lett., 21, 2935-2936 (1980)
A. Kraszewski and J. Stawinski
16. The case of sulfonation in the chemical synthesis of oligonucleotides
Nucleic Acids Res., 8, 2301-2305 (1980)
A. Kraszewski, J. Stawinski, and M. Wiewiorowski
15. Studies on Polynucleotide Synthesis
In: Phosphorus Chemistry Directed Towards Biology, ed. W. J. Stec, Pergamon Press, Oxford-New York, p. 9-12 (1980)
R. W. Adamiak, E. Biala, K. Grzeskowiak, R. Kierzek, W. T. Markiewicz, J. Stawinski, and M. Wiewiorowski
14. Method for the preparation of new derivatives of nucleosides
Polskie Biuro Patentowe, Patent Nr P-209 339, Sep. 2, 1978.
W. T. Markiewicz, R. W. Adamiak, K. Grzeskowiak, A. Kraszewski, J. Stawinski, M. Wiewiorowski, and J. Zarnowski
13. The chemical synthesis of anticodon loop of an eucaryotic intiator tRNA containing the hypermodified nucleoside t6A
Nucleic Acids Res., 5, 1889-1905 (1978)
R. W. Adamiak, E. Biala, K. Grzeskowiak, R. Kierzek, A. Kraszewski, W. T. Markiewicz, J. Okupniak, J. Stawinski, and M. Wiewiorowski
12. Minimal Length of Lactose Operator Sequence for the Specific Recognition by the Lactose Repressor
Proc. Natl. Acad. Sci. US, 74, 966-970 (1977)
C. P. Bahl, R. Wu, J. Stawinski, and S. A. Narang
11. Arylosulfonyltetrazoles as Condensing Reagents for Oligonucleotide Synthesis
Canadian Patent and Development Ltd., USA Patent Nr 4 059 592, Nov. 22,1977.
S. A. Narang and J. Stawinski
10. Arylosulfonyltetrazoles, new coupling reagents and further improvements in the triester method for the synthesis of deoxyribooligonucleotides
Nucleic Acids Res., 4, 353-371 (1977)
J. Stawinski, T. Hozumi, S. A. Narang, C. B. Bahl, and R. Wu
9. A Highly Effective Route to N,N-Disubstituted Ureas under Mild Conditions. An Application to the Synthesis of tRNA Anticodon Loop Fragments Containing Ureidonucloesides
Tetrahedron Lett., 1935-1936 (1977)
R. W. Adamiak and J. Stawinski
8. Nucleoside 3'-phosphotriester as a key intermediate for the oligonucleotide synthesis. IV. New method for removal of 2,2,2-trichloroethyl group and 31P NMR as a new tool for analysis of deblocking of internucleotide phosphate protecting groups
Nucleic Acids Res., 4, 2321-2329 (1977)
R. W. Adamiak, E. Biala, K. Grzeskowiak, R. Kierzek, A. Kraszewski, W. T. Markiewicz, J. Stawinski, and M. Wiewiorowski
7. Cloned Synthetic lac-Operator DNA is Biologically Active
Nature, 263, 744-748 (1976)
K. J. Marians, R. Wu, J. Stawinski, T. Hozumi, and S. A. Narang
6. Arylosulfonyltetrazoles as Highly Efficient Condensing Reagents for Polynucleotide Synthesis
Can. J. Chem., 54, 670-672 (1976)
J. Stawinski, T. Hozumi, and S. A. Narang
5. Benzoyltetrazole: a Mild Benzoylating Reagent for Nucleosides
J. Chem. Soc. Chem. Commun., 243-244 (1976)
J. Stawinski, T. Hozumi, and S. A. Narang
4. Chemical Synthesis of Deoxyribopolynucleotides
In: Structure, Synthesis and Properties of tRNA, ed. K. Grzeskowiak and J. Stawinski, Wydawnictwo UAM, Poznan, p. 28-40 (1976)
K. Grzeskowiak and J. Stawinski
3. A general method for inserting specific DNA sequences into cloning vehicles
Gene, 1, 81-92 (1976)
C. P. Bahl, K. J. Marians, R. Wu, J. Stawinski, and S. A. Narang
2. Collection of Methods and Reagents Used in the Synthesis of Nucleic Acid Components
In: Collection of methods and Reagents used in the Synthesis of Nucleic Acid Components, ed. P. Dembek, Wydawnictwo UAM, Poznan,    (1975)
R. W. Adamiak, J. Antkowiak, E. Biala, J. Boryski, P. Dembek, W. Folkman, W. Gessner, K. Grzeskowiak, R. Kierzek, A. Kraszewski, W. T. Markiewicz, J. Milecki, J. Okupniak, P. Serafinowski, J. Stawinski, and K. Weclawek
1. A New Example of the Protected Triester Nucleotide as a Key Intermediate for Synthesis of Oligomers
Bull. Acad. Pol. Sci. ser. chim., 23, 495-501 (1975)
K. Grzeskowiak, J. Stawinski, and M. Wiewiorowski