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Jacek Stawinski

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Chemicals & Drugs

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Co-Publications
Name
23
Kraszewski, Adam
13
Sobkowski, Michal
11
Strömberg, Roger
7
Jankowska, Jadwiga
5
Szymczak, Marzena
5
Kullberg, Martin
4
Johansson, Tommy
4
Nilsson, Johan
3
Szymanska, Agnieszka
3
Kulinska, K
3
Kalek, Marcin
3
Gosselin, Gilles
3
Imbach, Jean-Louis
3
Cieslak, Jacek
3
Boryski, Jerzy

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Publications

TOP 3
Romanowska Joanna; Szymanska-Michalak Agnieszka; Boryski Jerzy; Stawinski Jacek; Kraszewski Adam; Loddo Roberta; Sanna Giuseppina; Collu Gabriella; Secci Barbara; La Colla Paolo
Aryl nucleoside H-phosphonates. Part 16: synthesis and anti-HIV-1 activity of di-aryl nucleoside phosphotriesters.
Sobkowski Michal; Stawinski Jacek; Kraszewski Adam
A proposal for a convenient notation for P-chiral nucleotide analogues. Part 4. A relationship between the Dp/Lp notation and stereochemistry of reactions.
Kalek Marcin; Ziadi Asraa; Stawinski Jacek
Microwave-assisted palladium-catalyzed cross-coupling of aryl and vinyl halides with H-phosphonate diesters.

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All Publications

2009: Romanowska Joanna; Szymanska-Michalak Agnieszka; Boryski Jerzy; Stawinski Jacek; Kraszewski Adam; Loddo Roberta; Sanna Giuseppina; Collu Gabriella; Secci Barbara; La Colla Paolo
Aryl nucleoside H-phosphonates. Part 16: synthesis and anti-HIV-1 activity of di-aryl nucleoside phosphotriesters.
Bioorganic & medicinal chemistry 2009;17(9):3489-98.
2009: Sobkowski Michal; Stawinski Jacek; Kraszewski Adam
A proposal for a convenient notation for P-chiral nucleotide analogues. Part 4. A relationship between the Dp/Lp notation and stereochemistry of reactions.
Nucleosides, nucleotides & nucleic acids 2009;28(1):29-42.
2008: Kalek Marcin; Ziadi Asraa; Stawinski Jacek
Microwave-assisted palladium-catalyzed cross-coupling of aryl and vinyl halides with H-phosphonate diesters.
Organic letters 2008;10(20):4637-40.
2008: Bartoszewicz Agnieszka; Kalek Marcin; Stawinski Jacek
The case for the intermediacy of monomeric metaphosphate analogues during oxidation of H-phosphonothioate, H-phosphonodithioate, and H-phosphonoselenoate monoesters: mechanistic and synthetic studies.
The Journal of organic chemistry 2008;73(13):5029-38.
2008: Kalek Marcin; Bartoszewicz Agnieszka; Stawinski Jacek
Synthesis of nucleoside phosphorothio-, phosphorodithio- and phosphoroselenoate diesters via oxidative esterification of the corresponding H-phosphonate analogues.
Nucleic acids symposium series (2004) 2008;(52):285-6.
2007: Stamatov Stephan D; Stawinski Jacek
Regioselective and stereospecific acylation across oxirane- and silyloxy systems as a novel strategy to the synthesis of enantiomerically pure mono-, di- and triglycerides.
Organic & biomolecular chemistry 2007;5(23):3787-800.
2007: Sobkowski Michal; Stawinski Jacek; Kraszewski Adam
A convenient stereochemical notation for p-chiral nucleotide analogs.
Current protocols in nucleic acid chemistry / edited by Serge L. Beaucage ... [et al.] 2007;Appendix 1():Appendix 1E.
2006: Stamatov Stephan D; Stawinski Jacek
Regioselective and stereospecific cleavage of a terminal oxirane system: a novel synthetic approach to lipid mediator congeners--1,2(2,3)-diacyl-3(1)-halo-sn-glycerols.
Bioorganic & medicinal chemistry letters 2006;16(13):3388-91.
2006: Szymanska Agnieszka; Szymczak Marzena; Boryski Jerzy; Stawinski Jacek; Kraszewski Adam; Collu Gabriella; Sanna Giseppina; Giliberti Gabriele; Loddo Roberta; La Colla Paolo
Aryl nucleoside H-phosphonates. Part 15: Synthesis, properties and, anti-HIV activity of aryl nucleoside 5'-alpha-hydroxyphosphonates.
Bioorganic & medicinal chemistry 2006;14(6):1924-34.
2006: Sobkowski Michal; Stawinski Jacek; Kraszewski Adam
A proposal for a convenient notation for P-chiral nucleotide analogues. Part 3. Compounds with one nucleoside residue and nonnucleosidic derivatives.
Nucleosides, nucleotides & nucleic acids 2006;25(12):1377-89.
2006: Sobkowski Michal; Stawinski Jacek; Kraszewski Adam
A proposal for a convenient notation for P-chiral nucleotide analogues. Part 2. Dinucleoside monophosphate analogues.
Nucleosides, nucleotides & nucleic acids 2006;25(12):1363-75.
2006: Ji Sanhao; Ju Yong; Fu Hua; Zhao Yufen; Johansson Tommy; Stawinski Jacek
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 2006;25(7):771-84.
2005: Kullberg Martin; Stawinski Jacek
Preparation of nucleoside H-phosphonoselenoate monoesters via the phosphinate approach.
Nucleosides, nucleotides & nucleic acids 2005;24(10-12):1627-33.
2005: Sobkowski Michal; Jankowska Jadwiga; Kraszewski Adam; Stawinski Jacek
Stereochemistry of internucleotide bond formation by the H-phosphonate method. 1. Synthesis and 31P NMR analysis of 16 diribonulceoside (3'-5')-H-phosphonates and the corresponding phosphorothioates.
Nucleosides, nucleotides & nucleic acids 2005;24(10-12):1469-84.
2005: Sobkowski Michal; Stawinski Jacek; Kraszewski Adam
A proposal for a new stereochemical notation for P-chiral nucleotide analogues and related compounds.
Nucleosides, nucleotides & nucleic acids 2005;24(9):1301-7.
2005: Sobkowski Michal; Jankowska Jadwiga; Stawinski Jacek; Kraszewski Adam
A cautionary note on the use of the 31P NMR spectroscopy in stereochemical correlation analysis.
Nucleosides, nucleotides & nucleic acids 2005;24(5-7):1033-6.
2005: Sobkowski Michal; Jankowska Jadwiga; Stawinski Jacek; Kraszewski Adam
Aryl nucleoside H-phosphonates as a tool for investigation of stereospecificity during coupling.
Nucleosides, nucleotides & nucleic acids 2005;24(5-7):887-90.
2005: Kullberg Martin; Stawinski Jacek
Oxidative transformations of nucleoside fluorenemethyl H-phosphonoselenoate diesters.
Nucleosides, nucleotides & nucleic acids 2005;24(5-7):659-61.
2005: Johansson Tommy; Nilsson Johan; Kullberg Martin; Lavén Gaston; Sobkowski Michal; Szymanska Agnieszka; Szymczak Marzena; Kraszewski Adam; Stawinski Jacek
Developing synthetic methods for bioactive phosphorus compounds using H-phosphonate chemistry: a progress report.
Nucleosides, nucleotides & nucleic acids 2005;24(5-7):353-7.
2005: Stawinski Jacek; Strömberg Roger
Di- and oligonucleotide synthesis using H-phosphonate chemistry.
Methods in molecular biology (Clifton, N.J.) 2005;288():81-100.
2004: Strömberg Roger; Stawinski Jacek
Synthesis of oligodeoxyribo- and oligoribonucleotides according to the H-phosphonate method.
Current protocols in nucleic acid chemistry / edited by Serge L. Beaucage ... [et al.] 2004;Chapter 3():Unit 3.4.
2004: Nilsson Johan; Stawinski Jacek
Controlling stereochemistry during oxidative coupling. Preparation of Rp or Sp phosphoramidates from one P-chiral precursor.
Chemical communications (Cambridge, England) 2004;(22):2566-7.
2004: Almer Helena; Szabo Tomas; Stawinski Jacek
A new approach to stereospecific synthesis of P-chiral phosphorothioates. Preparation of diastereomeric dithymidyl-(3'-5') phosphorothioates.
Chemical communications (Cambridge, England) 2004;(3):290-1.
2003: Szymczak Marzena; Szymanska Agnieszka; Stawinski Jacek; Boryski Jerzy; Kraszewski Adam
Aryl h-phosphonates. 14. Synthesis of new nucleotide analogues with phosphonate-phosphate internucleosidic linkage.
Organic letters 2003;5(20):3571-3.
2003: Nilsson Johan; Kraszewski Adam; Stawinski Jacek
Chemoselectivity in oxidative coupling of bifunctional nucleophiles with dinucleoside H-phosphonate and dinucleoside H-phosphonothioate diesters.
Nucleosides, nucleotides & nucleic acids 2003;22(5-8):1467-9.
2003: Kullberg Martin; Stawinski Jacek
9-Fluorenemethyl H-phosphonoselenoate--a versatile reagent for transferring an H-phosphonoselenoate group.
Nucleosides, nucleotides & nucleic acids 2003;22(5-8):1463-5.
2003: Johansson Tommy; Stawinski Jacek
Studies towards synthesis of dinucleoside arylphosphonates with metal complexing properties.
Nucleosides, nucleotides & nucleic acids 2003;22(5-8):1459-61.
2003: Bollmark Martin; Johansson Tommy; Kullberg Martin; Nilsson Johan; Stawinski Jacek; Cieslak Jacek; Jankowska Jadwiga; Sobkowski Michal; Szymczak Marzena; Wenska Malgorzata; Kraszewski Adam
Developing synthetic methods for bioactive phosphorus compounds using H-phosphonate chemistry: a progress report.
Nucleosides, nucleotides & nucleic acids 2003;22(5-8):617-21.
2002: Stawinski Jacek; Kraszewski Adam
How to get the most out of two phosphorus chemistries. Studies on H-phosphonates.
Accounts of chemical research 2002;35(11):952-60.
2001: Golos B; Dzik J M; Kazimierczuk Z; Ciesla J; Zielinski Z; Jankowska J; Kraszewski A; Stawinski J; Rode W; Shugar D
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.
Biological chemistry 2001;382(10):1439-45.
2001: Johansson T; Stawinski J
The case for configurational stability of H-phosphonate diesters in the presence of diazabicyclo[5.4.0]undec-7-ene (DBU).
Bioorganic & medicinal chemistry 2001;9(9):2315-22.
2001: Stawinski J; Strömberg R
Deoxyribo- and ribonucleoside H-phosphonates.
Current protocols in nucleic acid chemistry / edited by Serge L. Beaucage ... [et al.] 2001;Chapter 2():Unit 2.6.
2001: Cieslak J; Sobkowski M; Jankowska J; Wenska M; Szymczak M; Imiolczyk B; Zagórowska I; Shugar D; Stawinski J; Kraszewski A
Nucleoside phosphate analogues of biological interest, and their synthesis via aryl nucleoside H-phosphonates as intermediates.
Acta biochimica Polonica 2001;48(2):429-42.
2000: Sobkowski M; Wenska M; Kraszewski A; Stawinski J
Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part VI. Reaction with diols.
Nucleosides, nucleotides & nucleic acids 2000;19(10-12):1487-503.
2000: Cieslak J; Jankowska J; Stawinski J; Kraszewski A
Aryl H-phosphonates. 12. Synthetic and (31)P NMR studies on the preparation of nucleoside H-phosphonothioate and nucleoside H-phosphonodithioate monoesters.
The Journal of organic chemistry 2000;65(21):7049-54.
1999: Kers I; Stawinski J; Girardet J L; Imbach J L; Périgaud C; Gosselin G; Aubertin A M
Synthesis and anti-retroviral activity of O,O'-bis(3'-azido-2',3'-dideoxythymidin-5'-yl) phosphoramidate derivatives.
Nucleosides & nucleotides 1999;18(10):2317-25.
1999: Kers I; Girardet J L; Gosselin G; Perigaud C; Imbach J L; Stawinski J
Synthesis and in vitro antiviral activity of some symmetrical phosphoramidate dimers of AZT.
Nucleosides & nucleotides 1999;18(4-5):993-4.
1998: Kulinska K; Kulinski T; Stawinski J; Laaksonen A
A molecular dynamics computer simulation study of nucleotide analogues. Comparison of the hydration pattern of dithymidine phosphate with those of the dithymidine methylphosphonate diastereomers.
Journal of biomolecular structure & dynamics 1998;15(5):987-98.
1998: Sobkowski M; Kraszewski A; Stawinski J
The reactions of H-phosphonates with bifunctional reagents. Part V. Functionalization of support-bound oligonucleotides and synthesis of non-radioactive hybridization probes.
Nucleosides & nucleotides 1998;17(1-3):253-67.
1998: Kulinska K; Kulinski T; Stawinski J
Hydration of C-H groups in natural dithymidine nucleotide and its methylphosphonate analogues.
Acta biochimica Polonica 1998;45(4):977-85.
1998: Stawinski J; Kraszewski A
Some aspects of oligoribonucleotides synthesis via the H-phosphonate approach.
Acta biochimica Polonica 1998;45(4):907-15.
1997: Kulinska K; Sarzynska J; Szabo T; Stawinski J
FTIR study on nucleotide analogues. 1. Spectral characterization of dinucleoside methylphosphonates and dinucleoside 5'-methylenephosphonates in solution and in solid phase.
Journal of biomolecular structure & dynamics 1997;15(1):119-28.
1996: Almer H; Stawinski J; Strömberg R
Solid support synthesis of all-Rp-oligo(ribonucleoside phosphorothioate)s.
Nucleic acids research 1996;24(19):3811-20.
1995: Szabó T; Kers A; Stawinski J
A new approach to the synthesis of the 5'-deoxy-5'-methylphosphonate linked thymidine oligonucleotide analogues.
Nucleic acids research 1995;23(6):893-900.
1993: Gosselin G; Périgaud C; Lefebvre I; Pompon A; Aubertin A M; Kirn A; Szabo T; Stawinski J; Imbach J L
5'-Hydrogenphosphonates of anti-HIV nucleoside analogues revisited: controversial mode of action.
Antiviral research 1993;22(2-3):143-53.
1993: Szabó T; Noréus D; Norrestam R; Stawinski J
Molecular and crystal structure of Sp-thymidin-3'-yl 4-thiothymidin-5'-yl methylphosphonate.
Nucleic acids research 1993;21(17):3921-6.
1991: Stawinski J; Strömberg R; Szabo T; Thelin M; Westman E; Zain R
Synthesis and some reactions of nucleoside H-phosphonothioate esters.
Nucleic acids symposium series 1991;(24):95-8.
1991: Stawinski J; Szabó T
Studies directed towards efficient synthesis of oligo-5'-deoxy-5-C-(phosphonomethyl)deoxyribonucleosides.
Nucleic acids symposium series 1991;(24):71-2.
1991: Stawinski J; Strömberg R; Zain R
Some chemical and stereochemical aspects of oxidation of nucleoside H-phosphonothioate diesters.
Nucleic acids symposium series 1991;(24):230.
1991: Stawinski J; Strömberg R; Szabó T
Convenient synthesis of dinucleotide methylphosphonates.
Nucleic acids symposium series 1991;(24):229.
1991: Stawinski J; Strömberg R; Westman E
Studies on reaction conditions for ribonucleotide synthesis via the H-phosphonate approach.
Nucleic acids symposium series 1991;(24):228.
1991: Almer H; Stawinski J; Strömberg R; Thelin M
Synthesis of diribonucleoside thiophosphates via stereospecific sulphurization of H-phosphonates.
Nucleic acids symposium series 1991;(24):227.
1989: Stawinski J; Szabó T; Thelin M; Westman E; Zain R
Recent studies on nucleoside H-phosphonothioate and nucleoside methylphosphonothioate synthesis.
Nucleic acids symposium series 1989;(21):47-8.
1988: Stawinski J; Strömberg R; Thelin M; Westman E
Studies on the t-butyldimethylsilyl group as 2'-O-protection in oligoribonucleotide synthesis via the H-phosphonate approach.
Nucleic acids research 1988;16(19):9285-98.
1987: Lindh I; Stawinski J
Synthesis of phospholipids and nucleoside-phospholipid conjugates via hydrogenphosphonate intermediates.
Nucleic acids symposium series 1987;(18):189-92.
1987: Strömberg R; Stawinski J
Evaluation of some new condensing reagents for hydrogenphosphonate diester formation.
Nucleic acids symposium series 1987;(18):185-8.
1984: Narang S A; Brousseau R; Georges F; Michniewicz J; Prefontaine G; Stawinski J; Sung W
The human preproinsulin gene: synthesis, cloning, gene modification, and expression studies.
Canadian journal of biochemistry and cell biology = Revue canadienne de biochimie et biologie cellulaire 1984;62(4):209-16.
1984: Georges F; Brousseau R; Michniewicz J; Prefontaine G; Stawinski J; Sung W; Wu R; Narang S A
Synthesis of a human insulin gene. VII. Synthesis of preproinsulin-like human DNA, its cloning and expression in M13 bacteriophage.
Gene 1984;27(2):201-11.
1982: Stawinski J
[Application of synthetic DNA fragments in molecular biology]
Postepy biochemii 1982;28(1-2):45-69.
1980: Kraszewski A; Stawinski J; Wiewiórowski M
The case of sulfonation in the chemical synthesis of oligonucleotides.
Nucleic acids research 1980;8(10):2301-5.
1980: Markiewicz W T; Biala E; Adamiak R W; Grzeskowiak K; Kierzek R; Kraszewski A; Stawinski J; Wiewiórowski M
Further studies on oligoribonucleotide synthesis.
Nucleic acids symposium series 1980;(7):115-27.
1978: Adamiak R W; Biala E; Grzeskowiak K; Kierzek R; Kraszewski A; Markiewicz W T; Okupniak J; Stawinski J; Wiewiórowski M
The chemical synthesis of the anticodon loop of an eukaryotic initiator tRNA containing the hypermodified nucleoside N6-/N-threonylcarbonyl/-adenosine/t6A/1.
Nucleic acids research 1978;5(6):1889-905.
1977: Adamiak R W; Biala E; Grzeskowiak; Kierzek R; Kraszewski A; Markiewicz W T; Stawinski J; Wiewiórowski
Nucleoside 3'-phosphotriesters as key intermediates for the oligoribonucleotide 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 research 1977;4(7):2321-9.
1977: Stawinski J; Hozumi T; Narang S A; Bahl C P; Wu R
Arylsulfonyltetrazoles, new coupling reagents and further improvements in the triester method for the synthesis of deoxyribooligonucleotides.
Nucleic acids research 1977;4(2):353-71.
1976: Marians K J; Wu R; Stawinski J; Hozumi T; Narang S A
Cloned synthetic lac operator DNA is biologically active.
Nature 1976;263(5580):744-8.

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