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Jacek Stawinski - Publications

Affiliations: 
1976-1984 Institute of Bio-Organic Chemistry, Polish Academy of Sciences 
 1984- Stockholm University, Stockholm, Stockholms län, Sweden 
Area:
Nucleic acid chemistry, bio-organic chemistry
Website:
http://www.organ.su.se/js/JS%20CV.html
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318 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Materna M, Stawiński J, Sobkowski M. A new approach to phosphorylation of nucleosides using oxyonium phosphobetaines as intermediates. Biotechnologia. 104: 93-99. PMID 37064278 DOI: 10.5114/bta.2022.120705  0.768
2023 Panda SS, Aziz MN, Stawinski J, Girgis AS. Azomethine Ylides-Versatile Synthons for Pyrrolidinyl-Heterocyclic Compounds. Molecules (Basel, Switzerland). 28. PMID 36677727 DOI: 10.3390/molecules28020668  0.353
2021 Gołębiewska J, Stawinski J. Correction to "Reaction of Boranephosphonate Diesters with Pyridines or Tertiary Amines in the Presence of Iodine: Synthetic and Mechanistic Studies". The Journal of Organic Chemistry. PMID 34846882 DOI: 10.1021/acs.joc.1c02582  0.74
2020 Kraszewski A, Sobkowski M, Stawinski J. H-Phosphonate Chemistry in the Synthesis of Electrically Neutral and Charged Antiviral and Anticancer Pronucleotides. Frontiers in Chemistry. 8: 595738. PMID 33282839 DOI: 10.3389/fchem.2020.595738  0.799
2020 Gołębiewska J, Stawinski J. Reaction of boranephosphonate diesters with pyridines or tertiary amines in the presence of iodine. Synthetic and mechanistic studies. The Journal of Organic Chemistry. PMID 32073846 DOI: 10.1021/Acs.Joc.9B03506  0.741
2018 Romanowska J, Kolodziej K, Sobkowski M, Rachwalak M, Jakubowski T, Golebiewska J, Kraszewski A, Boryski J, Dabrowska A, Stawinski J. Aryl H-phosphonates. 19. New anti-HIV pronucleotide phosphoramidate diesters containing amino- and hydroxypyridine auxiliaries. European Journal of Medicinal Chemistry. 164: 47-58. PMID 30590257 DOI: 10.1016/J.Ejmech.2018.12.038  0.813
2018 Gołębiewska J, Rachwalak M, Jakubowski T, Romanowska J, Stawinski J. Reaction of Boranephosphonate Diesters with Amines in the Presence of Iodine: The Case for the Intermediacy of H-Phosphonate Derivatives. The Journal of Organic Chemistry. PMID 29684279 DOI: 10.1021/Acs.Joc.8B00419  0.845
2017 Szymanska-Michalak A, Wawrzyniak D, Framski G, Stawinski J, Barciszewski J, Kraszewski A. New antiglioma zwitterionic pronucleotides with an FdUMP framework. European Journal of Medicinal Chemistry. 144: 682-691. PMID 29289891 DOI: 10.1016/J.Ejmech.2017.12.070  0.734
2016 Framski G, Wawrzyniak D, Jahnz-Wechmann Z, Szymanska-Michalak A, Kraszewski A, Barciszewski J, Boryski J, Stawinski J. Searching for anti-glioma activity. Ribonucleoside analogues with modifications in nucleobase and sugar moieties. Acta Biochimica Polonica. 63: 765-771. PMID 27830840 DOI: 10.18388/Abp.2016_1338  0.716
2016 Szymańska-Michalak A, Wawrzyniak D, Framski G, Kujda M, Zgoła P, Stawinski J, Barciszewski J, Boryski J, Kraszewski A. New 3'-O-aromatic acyl-5-fluoro-2'-deoxyuridine derivatives as potential anticancer agents. European Journal of Medicinal Chemistry. 115: 41-52. PMID 26994842 DOI: 10.1016/J.Ejmech.2016.03.010  0.772
2016 Materna M, Stawinski J, Kiliszek A, Rypniewski W, Sobkowski M. Oxyonium phosphobetaines – unusually stable nucleophilic catalyst–phosphate complexes formed from H-phosphonates and N-oxides Rsc Adv.. 6: 14448-14451. DOI: 10.1039/C5Ra27465F  0.8
2015 Kolodziej K, Romanowska J, Stawinski J, Boryski J, Dabrowska A, Lipniacki A, Piasek A, Kraszewski A, Sobkowski M. Aryl H-Phosphonates 18. Synthesis, properties, and biological activity of 2',3'-dideoxynucleoside (N-heteroaryl)phosphoramidates of increased lipophilicity. European Journal of Medicinal Chemistry. 100: 77-88. PMID 26071860 DOI: 10.1016/J.Ejmech.2015.06.004  0.805
2015 Wojdy?a-Mamo? AM, Zimny J, Romanowska J, Kraszewski A, Stawinski J, Bieganowski P, Guranowski A. Novel reactivity of Fhit proteins: catalysts for fluorolysis of nucleoside 5'-phosphoramidates and nucleoside 5'-phosphosulfates to generate nucleoside 5'-phosphorofluoridates. The Biochemical Journal. 468: 337-44. PMID 25826698 DOI: 10.1042/Bj20141568  0.739
2015 Kolodziej K, Romanowska J, Stawinski J, Kraszewski A, Sobkowski M. The case of triethylammonium cation loss during purification of certain nucleotide analogues: a cautionary note. Analytical and Bioanalytical Chemistry. 407: 1775-80. PMID 25542580 DOI: 10.1007/S00216-014-8397-0  0.789
2015 Sobkowski M, Kraszewski A, Stawinski J. Recent advances in H-phosphonate chemistry. Part 2. Synthesis of C-phosphonate derivatives. Topics in Current Chemistry. 361: 179-216. PMID 25391983 DOI: 10.1007/128_2014_563  0.84
2015 Sobkowski M, Kraszewski A, Stawinski J. Recent advances in H-phosphonate chemistry. Part 1. H-phosphonate esters: synthesis and basic reactions. Topics in Current Chemistry. 361: 137-77. PMID 25370520 DOI: 10.1007/128_2014_562  0.859
2015 Girgis AS, Mabied AF, Stawinski J, Hegazy L, George RF, Farag H, Shalaby EM, Farag ISA. Synthesis and DFT studies of an antitumor active spiro-oxindole New Journal of Chemistry. 39: 8017-8027. DOI: 10.1039/C5Nj01109D  0.366
2014 Kolodziej K, Kraszewski A, Stawinski J, Sobkowski M. The loss of TEAH + cation from certain nucleotide analogues Collection of Czechoslovak Chemical Communications. 14: 373-374. DOI: 10.1135/Css201414373  0.774
2014 Materna M, Stawinski J, Sobkowski M. Trialkylamine N -oxides as reagents in nucleotide chemistry Collection of Czechoslovak Chemical Communications. 14: 369-372. DOI: 10.1135/Css201414369  0.755
2014 Materna M, Stawinski J, Sobkowski M. N -Oxides as reagents in nucleotide chemistry Collection of Czechoslovak Chemical Communications. 14: 322-323. DOI: 10.1135/Css201414322  0.775
2013 George RF, Ismail NS, Stawinski J, Girgis AS. Design, synthesis and QSAR studies of dispiroindole derivatives as new antiproliferative agents. European Journal of Medicinal Chemistry. 68: 339-51. PMID 23994327 DOI: 10.1016/J.Ejmech.2013.07.035  0.44
2013 Rozniewska M, Stawinski J, Kraszewski A. Nucleoside 3',5'-cyclic H-phosphonates, new useful precursors for the synthesis of nucleoside 3',5'-cyclic phosphates and their analogues. Organic Letters. 15: 4082-5. PMID 23905847 DOI: 10.1021/Ol4016404  0.817
2012 Jiménez-Halla JO, Kalek M, Stawinski J, Himo F. Computational study of the mechanism and selectivity of palladium-catalyzed propargylic substitution with phosphorus nucleophiles. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 12424-36. PMID 22890875 DOI: 10.1002/Chem.201201026  0.844
2012 Girgis AS, Stawinski J, Ismail NS, Farag H. 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. European Journal of Medicinal Chemistry. 47: 312-22. PMID 22119131 DOI: 10.1016/J.Ejmech.2011.10.058  0.538
2012 Sobczak M, Johansson T, Bulkowski M, Sochacki M, Laven G, Mikolaczyk B, Stawinski J, Nawrot B. Dna oligonucleotides with stereodefined phenylphosphonate and phosphonothioate internucleotide bonds : synthesis and physico chemical properties Arkivoc. 2012: 63-79. DOI: 10.3998/Ark.5550190.0013.407  0.793
2012 Girgis AS, Stawinski J, Ismail NSM, Farag H. ChemInform Abstract: 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. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201224118  0.529
2011 Söderberg L, Lavén G, Kalek M, Stawinski J. 31P NMR and computational studies on stereochemistry of conversion of phosphoramidate diesters into the corresponding phosphotriesters. Nucleosides, Nucleotides & Nucleic Acids. 30: 552-64. PMID 21888546 DOI: 10.1080/15257770.2011.586009  0.804
2011 Romanowska J, Sobkowski M, Szymańska-Michalak A, Kołodziej K, Dąbrowska A, Lipniacki A, Piasek A, Pietrusiewicz ZM, Figlerowicz M, Guranowski A, Boryski J, Stawiński J, Kraszewski A. Aryl H-phosphonates 17: (N-aryl)phosphoramidates of pyrimidine nucleoside analogues and their synthesis, selected properties, and anti-HIV activity. Journal of Medicinal Chemistry. 54: 6482-91. PMID 21834513 DOI: 10.1021/Jm2001103  0.839
2011 Sobkowski M, Jankowska J, Stawiński J, Kraszewski A. Unusual Stereochemistry of Esterification of Uridine 3′-H-Phosphonothioate Phosphorus, Sulfur, and Silicon and the Related Elements. 186: 952-955. DOI: 10.1080/10426507.2010.503212  0.846
2011 Kalek M, Stawinski J. ChemInform Abstract: Novel, Stereoselective and Stereospecific Synthesis of Allenylphosphonates and Related Compounds via Palladium-Catalyzed Propargylic Substitution. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201150164  0.819
2011 Kalek M, Stawinski J. Novel, Stereoselective and Stereospecific Synthesis of Allenylphosphonates and Related Compounds via Palladium-Catalyzed Propargylic Substitution Advanced Synthesis & Catalysis. 353: 1741-1755. DOI: 10.1002/Adsc.201100119  0.869
2010 Kalek M, Johansson T, Jezowska M, Stawinski J. Palladium-catalyzed propargylic substitution with phosphorus nucleophiles: efficient, stereoselective synthesis of allenylphosphonates and related compounds. Organic Letters. 12: 4702-4. PMID 20853904 DOI: 10.1021/Ol102121J  0.83
2010 Sobkowski M, Stawinski J, Kraszewski A. 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. Nucleosides, Nucleotides & Nucleic Acids. 29: 628-45. PMID 20661816 DOI: 10.1080/15257770.2010.497014  0.86
2010 Stamatov SD, Stawinski J. O-Silylated C3-halohydrins as a novel class of protected building blocks for total, regio- and stereocontrolled synthesis of glycerolipid frameworks. Organic & Biomolecular Chemistry. 8: 463-77. PMID 20066285 DOI: 10.1039/B915533C  0.358
2010 Kalek M, Jezowska M, Stawinski J. Palladium-catalyzed propargylic substitution with phosphorus nucleophiles Synfacts. 2011: 307-307. DOI: 10.1055/S-0030-1259418  0.821
2010 Szymańska-Michalak A, Stawiński J, Kraszewski A. Studies on the decomposition pathways of diastereoisomeric mixtures of aryl nucleoside α-hydroxyphosphonates under hydrolytic conditions. Synthesis of α-hydroxyphosphonate monoesters New Journal of Chemistry. 34: 976. DOI: 10.1039/B9Nj00717B  0.778
2010 Lavén G, Kalek M, Jezowska M, Stawinski J. Preparation of benzylphosphonates via a palladium(0)-catalyzed cross-coupling of H-phosphonate diesters with benzyl halides. Synthetic and mechanistic studies New Journal of Chemistry. 34: 967. DOI: 10.1039/B9Nj00585D  0.853
2010 Sobkowski M, Stawinski J, Kraszewski A. Stereochemistry of internucleotide bond formation by the H-phosphonate method. 7. Stereoselective formation of ribonucleoside (RP)- and (SP)-3′-H-phosphonothioate monoesters Tetrahedron: Asymmetry. 21: 410-419. DOI: 10.1016/J.Tetasy.2010.01.022  0.859
2010 Laven G, Kalek M, Jezowska M, Stawinski J. ChemInform Abstract: Preparation of Benzylphosphonates via a Palladium(0)-Catalyzed Cross-Coupling of H-Phosphonate Diesters with Benzyl Halides. Synthetic and Mechanistic Studies. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201040191  0.844
2010 Kalek M, Jezowska M, Stawinski J. ChemInform Abstract: Preparation of Arylphosphonates by Palladium(0)-Catalyzed Cross-Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic Studies. Cheminform. 41. DOI: 10.1002/CHIN.201019169  0.805
2010 Kalek M, Stawinski J. ChemInform Abstract: Efficient Synthesis of Mono- and Diarylphosphinic Acids: A Microwave-Assisted Palladium-Catalyzed Cross-Coupling of Aryl Halides with Phosphinate. Cheminform. 41. DOI: 10.1002/CHIN.201014172  0.809
2010 Romanowska J, Szymanska-Michalak A, Pietkiewicz M, Sobkowski M, Boryski J, Stawinski J, Kraszewski A. ChemInform Abstract: A New, Efficient Entry to Non-lipophilic H-Phosphonate Monoesters - Preparation of anti-HIV Nucleotide Analogues. Cheminform. 41. DOI: 10.1002/CHIN.201007199  0.82
2010 Sobkowski M, Wenska M, Kraszewski A, Stawinski J. ChemInform Abstract: Studies on Reactions of Nucleoside H-Phosphonates with Bifunctional Reagents. Part 6. Reaction with Diols. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200220182  0.812
2010 Cieslak J, Jankowska J, Sobkowski M, Wenska M, Stawinski J, Kraszewski A. ChemInform Abstract: Aryl H-Phosphonates. Part 13. A New, General Entry to Aryl Nucleoside Phosphate and Aryl Nucleoside Phosphorothioate Diesters. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200220174  0.839
2010 Johansson T, Stawinski J. ChemInform Abstract: Synthesis of Dinucleoside Pyridylphosphonates Involving Palladium(0)-Catalyzed Phosphorus-Carbon Bond Formation as a Key Step. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200216203  0.78
2010 Wenska M, Jankowska J, Sobkowski M, Stawinski J, Kraszewski A. ChemInform Abstract: A New Method for the Synthesis of Nucleoside 2′,3′-O,O-Cyclic Phosphorodithioates via Aryl Cyclic Phosphites as Intermediates. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200209225  0.77
2010 Cieslak J, Sobkowski M, Jankowska J, Wenska M, Szymczak M, Imiolczyk B, Zagorowska I, Shugar D, Stawinski J, Kraszewski A. ChemInform Abstract: Nucleoside Phosphate Analogues of Biological Interest, and Their Synthesis via Aryl Nucleoside H-Phosphonates as Intermediates. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200201296  0.865
2010 Bollmark M, Stawinski J. ChemInform Abstract: A New Selenium-Transferring Reagent - Triphenylphosphine Selenide. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200132216  0.696
2010 Johansson T, Kers A, Stawinski J. ChemInform Abstract: 2-Pyridylphosphonates: A New Type of Modification for Nucleotide Analogues. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200126213  0.757
2010 Jankowska J, Wenska M, Popenda M, Stawinski J, Kraszewski A. ChemInform Abstract: A New, Efficient Entry to Nucleoside 2′,3′-O,O-Cyclophosphorothioates. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200026209  0.274
2010 Kers I, Stawinski J, Girardet J, Imbach J, Perigaud C, Gosselin G, Aubertin A. ChemInform Abstract: Synthesis and Antiretroviral Activity of O,O′-Bis(3′-azido-2′,3′-dideoxythymidin-5′-yl) Phosphoramidate Derivatives. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200011227  0.356
2010 Misiura K, Bollmark M, Stawinski J, Stec WJ. ChemInform Abstract: Studies on Enzymatic Hydrolysis of Thymidin-3′-yl Thymidin-5′-yl Phosphorofluoridates and the Corresponding Phosphorothiofluoridates. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200005251  0.731
2010 Kers I, Stawinski J, Kraszewski A. ChemInform Abstract: Aryl H-Phosphonates. Part 10. Synthesis of Nucleoside Phosphoramidate and Nucleoside Phosphoramidothioate Analogues via H-Phosphonamidate Intermediates. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200002230  0.57
2010 Kers A, Szabo T, Stawinski J. ChemInform Abstract: Preparation of Nucleoside 5′-Deoxy-5′-methylenephosphonates as Building Blocks for the Synthesis of Methylenephosphonate Analogues. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200001231  0.373
2010 Kers A, Dembkowski L, Kraszewski A, Stawinski J. ChemInform Abstract: Studies on the Reaction of Trityl Derivatives with H-Phosphonate Diesters: Their Relevance to the Synthesis of 4-Pyridylphosphonates. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199952180  0.557
2010 Kers I, Cieslak J, Jankowska J, Kraszewski A, Stawinski J. ChemInform Abstract: New Methods for Multiple Modifications of a Phosphorus Center. Their Relevance to Nucleotide and Oligonucleotide Analogues Synthesis Cheminform. 30: no-no. DOI: 10.1002/CHIN.199943236  0.39
2010 Bollmark M, Stawinski J. ChemInform Abstract: A Mild Method for the Preparation of Nucleoside Phosphorofluoridate and Phosphorofluoridothioate Diesters Cheminform. 30: no-no. DOI: 10.1002/CHIN.199943235  0.721
2010 Stawinski J, Kraszewski A. ChemInform Abstract: Some Aspects of Oligoribonucleotides Synthesis via the H-Phosphonate Approach Cheminform. 30: no-no. DOI: 10.1002/CHIN.199930297  0.808
2010 Jankowska J, Sobkowska A, Cieslak J, Sobkowski M, Kraszewski A, Stawinski J, Shugar D. ChemInform Abstract: Nucleoside H-Phosphonates. Part 18. Synthesis of Unprotected Nucleoside 5′-H-Phosphonates and Nucleoside 5′-H-Phosphonothioates and Their Conversion into the 5′-Phosphorothioate and 5′-Phosphorodithioate Monoesters. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199914261  0.839
2010 BOLLMARK M, STAWINSKI J. ChemInform Abstract: Nucleotide Analogues Containing the P-F Bond. An Overview of the Synthetic Methods. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199827332  0.705
2010 KERS A, STAWINSKI J, DEMBKOWSKI L, KRASZEWSKI A. ChemInform Abstract: Aryl H-Phosphonates. Part 7. Studies on the Formation of Phosphorus-Carbon Bond in the Reaction of Trityl and Benzyl Halides with Dialkyl and Diphenyl H-Phosphonates. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199801194  0.512
2010 BOLLMARK M, KERS A, KERS I, SZABO T, ZAIN R, STAWINSKI J, CIESLAK J, JANKOWSKA J, KRASZEWSKI A. ChemInform Abstract: Studies on Nucleoside Phosphonates and Their Derivatives. A Progress Report Cheminform. 28: no-no. DOI: 10.1002/CHIN.199748298  0.794
2010 BOLLMARK M, STAWINSKI J. ChemInform Abstract: A New Method for the Formation of the P-F Bond. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199741273  0.701
2010 JANKOWSKA J, CIESLAK J, KRASZEWSKI A, STAWINSKI J. ChemInform Abstract: 9-Fluorenemethyl H-Phosphonothioate, a Versatile Reagent for the Preparation of H-Phosphonothioate, Phosphorothioate, and Phosphorodithioate Monoesters. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199728180  0.525
2010 BOLLMARK M, STAWINSKI J. ChemInform Abstract: A Facile Access to Nucleoside Phosphorofluoridate, Nucleoside Phosphorofluoridothioate, and Nucleoside Phosphorofluoridodithioate Monoesters. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199646260  0.716
2010 STAWINSKI J, STROEMBERG R. ChemInform Abstract: H-Phosphonates in Oligonucleotide Synthesis Cheminform. 27: no-no. DOI: 10.1002/chin.199642265  0.553
2010 KERS A, KERS I, KRASZEWSKI A, SOBKOWSKI M, SZABO T, THELIN M, ZAIN R, STAWINSKI J. ChemInform Abstract: Nucleoside Phosphonates. Development of Synthetic Methods and Reagents Cheminform. 27: no-no. DOI: 10.1002/chin.199625321  0.802
2010 KERS A, KERS I, STAWINSKI J, SOBKOWSKI M, KRASZEWSKI A. ChemInform Abstract: Studies on Aryl H-Phosphonates. Part 2. A General Method for the Preparation of Alkyl H-Phosphonate Monoesters. Cheminform. 26: no-no. DOI: 10.1002/chin.199544187  0.841
2010 SZABO T, KERS A, STAWINSKI J. ChemInform Abstract: Solid Phase Synthesis of 5′-Methylenephosphonate DNA Cheminform. 26: no-no. DOI: 10.1002/chin.199539257  0.293
2010 JANKOWSKA J, SOBKOWSKI M, STAWINSKI J, KRASZEWSKI A. ChemInform Abstract: Studies on Aryl H-Phosphonates. Part 1. An Efficient Method for the Preparation of Deoxyribo- and Ribonucleoside 3′-H-phosphonate Monoesters by Transesterification of Diphenyl H-Phosphonate. Cheminform. 25: no-no. DOI: 10.1002/chin.199438269  0.84
2010 STAWINSKI J, THELIN M. ChemInform Abstract: Nucleoside H-Phosphonates. Part 14. Synthesis of Nucleoside Phosphoroselenoates and Phosphorothioselenoates via Stereospecific Selenization of the Corresponding H-Phosphonate and H-Phosphonothioate Diesters with the Aid of New Seleniu Cheminform. 25: no-no. DOI: 10.1002/chin.199423236  0.546
2010 STAWINSKI J, THELIN M. ChemInform Abstract: 3H-1,2-Benzothiaselenol-3-one. A New Selenizing Reagent for Nucleoside H-Phosphonate and H-Phosphonothioate Diesters. Cheminform. 24: no-no. DOI: 10.1002/chin.199316272  0.515
2010 STAWINSKI J. ChemInform Abstract: Some Aspects of H-Phosphonate Chemistry Cheminform. 24: no-no. DOI: 10.1002/chin.199315332  0.517
2010 ALMER H, STAWINSKI J, STROEMBERG R, THELIN M. ChemInform Abstract: Synthesis of Diribonucleoside Phosphorothioates via Stereospecific Sulfurization of H-Phosphonate Diesters. Cheminform. 24: no-no. DOI: 10.1002/chin.199310275  0.555
2010 STAWINSKI J, THELIN M. ChemInform Abstract: 3-H-2,1-Benzoxathiol-3-one 1-Oxide. A New Reagent for Stereospecific Oxidation of Nucleoside H-Phosphonothioate Diesters, e.g. (I). Cheminform. 23: no-no. DOI: 10.1002/chin.199247255  0.424
2010 STAWINSKI J, STROEMBERG R, ZAIN R. ChemInform Abstract: Stereospecific Oxidation and Oxidative Coupling of H-Phosphonate and H- Phosphonothioate Diesters. Cheminform. 23: no-no. DOI: 10.1002/chin.199247254  0.726
2010 STAWINSKI J, THELIN M. ChemInform Abstract: Nucleoside H-Phosphonates. Part 13. Studies on 3H-1,2-Benzodithiol-3- one Derivatives as Sulfurizing Reagents for H-Phosphonate and H- Phosphonothioate Diesters. Cheminform. 23: no-no. DOI: 10.1002/chin.199204096  0.516
2009 Romanowska J, Szymańska-Michalak A, Boryski J, Stawiński J, Kraszewski A, Loddo R, Sanna G, Collu G, Secci B, La Colla P. Aryl nucleoside H-phosphonates. Part 16: synthesis and anti-HIV-1 activity of di-aryl nucleoside phosphotriesters. Bioorganic & Medicinal Chemistry. 17: 3489-98. PMID 19282192 DOI: 10.1016/J.Bmc.2009.02.033  0.782
2009 Sobkowski M, Stawinski J, Kraszewski A. 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. 28: 29-42. PMID 19116868 DOI: 10.1080/15257770802581724  0.808
2009 Romanowska J, Szymanska-Michalak A, Pietkiewicz M, Sobkowski M, Boryski J, Stawinski J, Kraszewski A. A New, Efficient Entry to Non-Lipophilic H-Phosphonate Monoesters – Preparation of Anti-HIV Nucleotide Analogues Letters in Organic Chemistry. 6: 496-499. DOI: 10.2174/157017809789124821  0.84
2009 Wallin R, Kalek M, Bartoszewicz A, Thelin M, Stawinski J. On the sulfurization of h-phosphonate diesters and phosphite triesters using elemental sulfur Phosphorus, Sulfur and Silicon and the Related Elements. 184: 908-916. DOI: 10.1080/10426500802715619  0.838
2009 Stawinski J, Lavén G. Palladium(0)-Catalyzed Benzylation of H-Phosphonate Diesters: An Efficient Entry to Benzylphosphonates Synlett. 2009: 225-228. DOI: 10.1055/S-0028-1087522  0.839
2009 Sobkowski M, Stawinski J, Kraszewski A. The role of nucleophilic catalysis in chemistry and stereochemistry of ribonucleosideH-phosphonate condensation New J. Chem.. 33: 164-170. DOI: 10.1039/B812780H  0.847
2009 Kalek M, Stawinski J. Efficient synthesis of mono- and diarylphosphinic acids: a microwave-assisted palladium-catalyzed cross-coupling of aryl halides with phosphinate Tetrahedron. 65: 10406-10412. DOI: 10.1016/J.Tet.2009.10.028  0.806
2009 Laven G, Stawinski J. ChemInform Abstract: Palladium(0)-Catalyzed Benzylation of H-Phosphonate Diesters: An Efficient Entry to Benzylphosphonates. Cheminform. 40. DOI: 10.1002/chin.200922173  0.541
2009 Kalek M, Jezowska M, Stawinski J. Preparation of Arylphosphonates by Palladium(0)-Catalyzed Cross-Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic Studies Advanced Synthesis & Catalysis. 351: 3207-3216. DOI: 10.1002/Adsc.200900590  0.816
2008 Kalek M, Ziadi A, Stawinski J. Microwave-assisted palladium-catalyzed cross-coupling of aryl and vinyl halides with H-phosphonate diesters. Organic Letters. 10: 4637-40. PMID 18808138 DOI: 10.1021/Ol801935R  0.838
2008 Kalek M, Bartoszewicz A, Stawinski J. Synthesis of nucleoside phosphorothio-, phosphorodithio- and phosphoroselenoate diesters via oxidative esterification of the corresponding H-phosphonate analogues. Nucleic Acids Symposium Series (2004). 285-6. PMID 18776365 DOI: 10.1135/Css200810219  0.866
2008 Bartoszewicz A, Kalek M, Stawinski J. 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. 73: 5029-38. PMID 18507440 DOI: 10.1021/Jo8006072  0.843
2008 Lavén G, Stawinski J. Synthetic studies on nucleoside 5'-H-phosphonate monoesters under Mitsunobu reaction conditions Arkivoc. 2009. DOI: 10.3998/Ark.5550190.0010.304  0.811
2008 Lavén G, Stawinski J. A new synthetic route to diastereomerically pure P-chiral nucleotide analogues, dinucleoside benzylphosphonates, via stereospecific Pd(0) catalyzed cross-coupling reaction Collection of Czechoslovak Chemical Communications. 10: 395-397. DOI: 10.1135/Css200810395  0.76
2008 Kalek M, Stawinski J. 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 of Czechoslovak Chemical Communications. 10: 214-218. DOI: 10.1135/Css200810214  0.815
2008 Bartoszewicz A, Kalek M, Nilsson J, Hiresova R, Stawinski J. A new reagent system for efficient silylation of alcohols: Silyl chloride-N-methylimidazole-iodine Synlett. 0037-0040. DOI: 10.1055/S-2007-992379  0.787
2008 Kalek M, Stawinski J. Palladium-Catalyzed C−P Bond Formation: Mechanistic Studies on the Ligand Substitution and the Reductive Elimination. An Intramolecular Catalysis by the Acetate Group in PdIIComplexes Organometallics. 27: 5876-5888. DOI: 10.1021/Om800641N  0.796
2008 Sobkowski M, Stawinski J, Kraszewski A. Stereochemistry of internucleotide bond formation by the H-phosphonate method. Part 6: Optimization of the reaction conditions towards highest stereoselectivity Tetrahedron: Asymmetry. 19: 2508-2518. DOI: 10.1016/J.Tetasy.2008.11.002  0.827
2008 Bartoszewicz A, Kalek M, Stawinski J. Iodine-promoted silylation of alcohols with silyl chlorides. Synthetic and mechanistic studies Tetrahedron. 64: 8843-8850. DOI: 10.1016/J.Tet.2008.06.070  0.774
2008 Stamatov SD, Stawinski J. Regioselective and Stereospecific Halosilylating Cleavage of the Oxirane System of Glycidol Derivatives as an Efficient Strategy to C2-O-Functionalized C3-Vicinal Halohydrins European Journal of Organic Chemistry. 2008: 2635-2643. DOI: 10.1002/Ejoc.200800112  0.418
2008 Bartoszewicz A, Kalek M, Stawinski J. ChemInform Abstract: Iodine-Promoted Silylation of Alcohols with Silyl Chlorides. Synthetic and Mechanistic Studies. Cheminform. 39. DOI: 10.1002/CHIN.200852047  0.776
2008 Bartoszewicz A, Kalek M, Nilsson J, Hiresova R, Stawinski J. ChemInform Abstract: A New Reagent System for Efficient Silylation of Alcohols: Silyl Chloride-N-Methylimidazole-Iodine. Cheminform. 39. DOI: 10.1002/CHIN.200820041  0.783
2007 Sobkowski M, Stawinski J, Kraszewski A. A convenient stereochemical notation for p-chiral nucleotide analogs. Current Protocols in Nucleic Acid Chemistry. Appendix 1E. PMID 18428960 DOI: 10.1002/0471142700.Nca01Es28  0.779
2007 Stamatov SD, Stawinski J. 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. 5: 3787-800. PMID 18004458 DOI: 10.1039/B713246H  0.478
2007 Kraszewski A, Stawinski J. H-Phosphonates: Versatile synthetic precursors to biologically active phosphorus compounds Pure and Applied Chemistry. 79: 2217-2227. DOI: 10.1351/Pac200779122217  0.819
2007 Stawinski J, Hiresova R. Nucleoside H-Phosphonates, XXII: Synthesis and Properties of New Nucleotide Analogues - H-Phosphonothiolate Diesters Synlett. 2007: 2748-2752. DOI: 10.1055/S-2007-991072  0.603
2007 Stamatov S, Stawinski J. Direct Trifluoroacetylation Across a Trimethylsilyloxy System as a Stereo­specific, Chemo- and Regioselective Approach to C3-Vicinal Halohydrins Synlett. 2007: 0439-0442. DOI: 10.1055/S-2007-968031  0.342
2007 Kalek M, Stawinski J. 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. DOI: 10.1021/Om700797K  0.778
2007 Stamatov SD, Stawinski J. Regioselective and stereospecific opening of an oxirane system mediated by trifluoroacetic acid and halide anions. A new direct approach to C3-vicinal halohydrins Tetrahedron Letters. 48: 1887-1889. DOI: 10.1016/J.Tetlet.2007.01.083  0.425
2007 Sobkowski M, Kraszewski A, Stawinski J. Stereochemistry of internucleotide bond formation by the H-phosphonate method. Part 3: Investigations on a mechanism of asymmetric induction Tetrahedron: Asymmetry. 18: 2336-2348. DOI: 10.1016/J.Tetasy.2007.09.017  0.829
2006 Sobkowski M, Stawinski J, Kraszewski A. 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. 25: 1377-89. PMID 17067959 DOI: 10.1080/15257770600918888  0.8
2006 Sobkowski M, Stawinski J, Kraszewski A. A proposal for a convenient notation for P-chiral nucleotide analogues. Part 2. Dinucleoside monophosphate analogues. Nucleosides, Nucleotides & Nucleic Acids. 25: 1363-75. PMID 17067958 DOI: 10.1080/15257770600918862  0.81
2006 Ji S, Ju Y, Fu H, Zhao Y, Johansson T, Stawinski J. 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: 771-84. PMID 16898415 DOI: 10.1080/15257770600726067  0.757
2006 Stamatov SD, Stawinski J. 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. 16: 3388-91. PMID 16677811 DOI: 10.1016/J.Bmcl.2006.04.040  0.431
2006 Szymańska A, Szymczak M, Boryski J, Stawiński J, Kraszewski A, Collu G, Sanna G, Giliberti G, Loddo R, La Colla P. Aryl nucleoside H-phosphonates. Part 15: Synthesis, properties and, anti-HIV activity of aryl nucleoside 5'-alpha-hydroxyphosphonates. Bioorganic & Medicinal Chemistry. 14: 1924-34. PMID 16290162 DOI: 10.1016/J.Bmc.2005.10.048  0.776
2006 Nilsson J, Szabo T, Laven G, Kullberg M, Kraszewski A, Stawinski J. Developing Synthetic Methods for Bioactive Phosphorus Compounds: A Progress Report Cheminform. 37. DOI: 10.1135/Css200507189  0.787
2006 Bollmark M, Kullberg M, Stawinski J. Studies on Oxidative Transformations of Dinucleoside H-Phosphonoselenoates. Cheminform. 37. DOI: 10.1135/Cccc20060832  0.846
2006 Bollmark M, Kullberg M, Stawinski J. Studies on Oxidative Transformations of Dinucleoside H-Phosphonoselenoates Collection of Czechoslovak Chemical Communications. 71: 832-841. DOI: 10.1135/CCCC20060832  0.846
2006 Kullberg M, Bollmark M, Stawinski J. Nucleoside H-Phosphonates. XXI. Synthetic and 31P NMR Studies on the Preparation of Dinucleoside H-Phosphonoselenoates Collection of Czechoslovak Chemical Communications. 71: 820-831. DOI: 10.1135/Cccc20060820  0.865
2006 Stamatov S, Stawinski J. Regioselective, Haloacylating Cleavage of an Oxirane System Mediated by Trifluoroacetic Anhydride/Trimethylsilyl Halides: An Efficient Entry to 2-Acyl-3-haloglycerols Synlett. 2006: 2251-2255. DOI: 10.1055/S-2006-948206  0.442
2006 Stamatov SD, Stawinski J. Efficient, highly regioselective, and stereospecific conversion of glycidol systems into C2-O-acylated vicinal halohydrins Tetrahedron Letters. 47: 2543-2547. DOI: 10.1016/J.Tetlet.2006.02.050  0.42
2005 Kullberg M, Stawinski J. Preparation of nucleoside H-phosphonoselenoate monoesters via the phosphinate approach. Nucleosides, Nucleotides & Nucleic Acids. 24: 1627-33. PMID 16438039 DOI: 10.1080/15257770500266883  0.853
2005 Sobkowski M, Jankowska J, Kraszewski A, Stawinski J. 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. 24: 1469-84. PMID 16438029 DOI: 10.1080/15257770500265729  0.857
2005 Sobkowski M, Stawinski J, Kraszewski A. A proposal for a new stereochemical notation for P-chiral nucleotide analogues and related compounds. Nucleosides, Nucleotides & Nucleic Acids. 24: 1301-7. PMID 16252667 DOI: 10.1080/15257770500230392  0.798
2005 Sobkowski M, Jankowska J, Stawinski J, Kraszewski A. A cautionary note on the use of the 31P NMR spectroscopy in stereochemical correlation analysis. Nucleosides, Nucleotides & Nucleic Acids. 24: 1033-6. PMID 16248086 DOI: 10.1081/Ncn-200059759  0.832
2005 Sobkowski M, Jankowska J, Stawinski J, Kraszewski A. Aryl nucleoside H-phosphonates as a tool for investigation of stereospecificity during coupling. Nucleosides, Nucleotides & Nucleic Acids. 24: 887-90. PMID 16248055 DOI: 10.1081/Ncn-200059239  0.85
2005 Kullberg M, Stawinski J. Oxidative transformations of nucleoside fluorenemethyl H-phosphonoselenoate diesters. Nucleosides, Nucleotides & Nucleic Acids. 24: 659-61. PMID 16248008 DOI: 10.1081/Ncn-200060173  0.774
2005 Johansson T, Nilsson J, Kullberg M, Lavén G, Sobkowski M, Szymanska A, Szymczak M, Kraszewski A, Stawinski J. Developing synthetic methods for bioactive phosphorus compounds using H-phosphonate chemistry: a progress report. Nucleosides, Nucleotides & Nucleic Acids. 24: 353-7. PMID 16247951 DOI: 10.1081/Ncn-200059778  0.842
2005 Stawinski J, Strömberg R. Di- and oligonucleotide synthesis using H-phosphonate chemistry. Methods in Molecular Biology (Clifton, N.J.). 288: 81-100. PMID 15333899 DOI: 10.1385/1-59259-823-4:081  0.754
2005 Nilsson J, Kraszewski A, Stawinski J. Chemical and Stereochemical Aspects of Oxidative Coupling of HPhosphonate and H-Phosphonothioate Diesters. Reactions with N,N-, N,Oand O,O-Binucleophiles Letters in Organic Chemistry. 2: 188-197. DOI: 10.2174/1570178053202937  0.844
2005 Sobkowski M, Stawinski J, Kraszewski A. A proposal of D P / L P notation for nucleotide analogues with a chiral phosphorus centre Collection of Czechoslovak Chemical Communications. 7: 467-469. DOI: 10.1135/Css200507467  0.776
2005 Kullberg M, Stawinski J. Reactions of H-phosphonate and H-phosphonothioate diesters with carbonyl compounds. 31 P NMR studies Collection of Czechoslovak Chemical Communications. 7: 207-211. DOI: 10.1135/Css200507207  0.838
2005 Hiresova R, Putilova L, Kullberg M, Stawinski J. Determination of absolute configuration of nucleoside 3'-H-phosphonothioate monoesters via stereochemical correlation analysis Collection of Czechoslovak Chemical Communications. 7: 201-205. DOI: 10.1135/Css200507201  0.81
2005 Lavén G, Stawinski J. Synthetic studies on the preparation of dinucleoside phenylphosphonates and phenylphosphonothioates via palladium(0) catalysed cross-coupling Collection of Czechoslovak Chemical Communications. 7: 195-199. DOI: 10.1135/Css200507195  0.743
2005 Sobkowski M, Jankowska J, Stawinski J, Kraszewski A. Stereochemistry of internucleotide bond formation by the H -phosphonate method. 2. Transesterification of aryl ribonucleoside H -phosphonate diesters with alcohols Collection of Czechoslovak Chemical Communications. 7: 183-187. DOI: 10.1135/Css200507183  0.837
2005 Stamatov SD, Stawinski J. Direct acylation across a silyloxy system of glycerol with carboxylic acid anhydrides : A novel strategy to the prodrug carrier modules - 1,3-diacyl-sn-glycerols Synlett. 2005: 2587-2590. DOI: 10.1055/S-2005-917084  0.433
2005 Kullberg M, Stawinski J. Nucleoside H-Phosphonates XX. Efficient Method for the Preparation of Nucleoside H-Phosphonoselenoate Monoesters Synthesis. 2005: 1668-1674. DOI: 10.1055/S-2005-865300  0.825
2005 Stamatov SD, Kullberg M, Stawinski J. 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 Letters. 46: 6855-6859. DOI: 10.1016/J.Tetlet.2005.08.015  0.757
2005 Stamatov SD, Stawinski J. 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 Letters. 46: 1601-1605. DOI: 10.1016/J.Tetlet.2005.01.093  0.485
2005 Stamatov SD, Stawinski J. 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. DOI: 10.1016/J.Tet.2005.02.034  0.474
2005 Kullberg M, Stawinski J. Theoretical investigations on the mechanism of chalcogens exchange reaction between P(V) and P(III) compounds Journal of Organometallic Chemistry. 690: 2571-2576. DOI: 10.1016/J.Jorganchem.2004.10.026  0.758
2005 Kraszewski A, Stawinski J. Aryl Nucleoside H-Phosphonates: Versatile Intermediates in the Synthesis of Nucleotides and Their Analogues Cheminform. 36. DOI: 10.1002/CHIN.200550256  0.83
2004 Strömberg R, Stawinski J. Synthesis of oligodeoxyribo- and oligoribonucleotides according to the H-phosphonate method. Current Protocols in Nucleic Acid Chemistry. Unit 3.4. PMID 18428927 DOI: 10.1002/0471142700.Nc0304S19  0.758
2004 Nilsson J, Stawinski J. Controlling stereochemistry during oxidative coupling. Preparation of Rp or Sp phosphoramidates from one P-chiral precursor. Chemical Communications (Cambridge, England). 2566-7. PMID 15543282 DOI: 10.1039/B411451E  0.62
2004 Almer H, Szabo T, Stawinski J. A new approach to stereospecific synthesis of P-chiral phosphorothioates. Preparation of diastereomeric dithymidyl-(3'-5') phosphorothioates. Chemical Communications (Cambridge, England). 290-1. PMID 14740042 DOI: 10.1039/B311912B  0.795
2004 Guimarāes R, Pasian S, Padilha I, Bidóia R, Stawinski J, Limissuri I, Passos M, Mársico R, Name C. Des formes reticulees de presentation echographique des hepatites virales Journal De Radiologie. 85: 1382. DOI: 10.1016/S0221-0363(04)77239-X  0.197
2004 Johansson T, Stawinski J. Nucleoside H-phosphonates. Part 19: Efficient entry to novel nucleotide analogues with 2-pyridyl- and 4-pyridylphosphonothioate internucleotide linkages Tetrahedron. 60: 389-395. DOI: 10.1016/J.Tet.2003.11.010  0.833
2004 Lavén G, Nilsson J, Stawinski J. Silylation-Mediated Transesterification ofO-Phenyl H-Phosphonothioates − A New Entry to Nucleoside H-Phosphonothioate Monoesters European Journal of Organic Chemistry. 2004: 5111-5224. DOI: 10.1002/Ejoc.200400550  0.843
2004 Szymczak M, Szymanska A, Stawinski J, Boryski J, Kraszewski A. Aryl H-Phosphonates. Part 14. Synthesis of New Nucleotide Analogues with Phosphonate—Phosphate Internucleosidic Linkage. Cheminform. 35. DOI: 10.1002/CHIN.200403204  0.549
2003 Nilsson J, Kraszewski A, Stawinski J. Chemoselectivity in oxidative coupling of bifunctional nucleophiles with dinucleoside H-phosphonate and dinucleoside H-phosphonothioate diesters. Nucleosides, Nucleotides & Nucleic Acids. 22: 1467-9. PMID 14565444 DOI: 10.1081/Ncn-120023012  0.838
2003 Kullberg M, Stawinski J. 9-Fluorenemethyl H-phosphonoselenoate--a versatile reagent for transferring an H-phosphonoselenoate group. Nucleosides, Nucleotides & Nucleic Acids. 22: 1463-5. PMID 14565443 DOI: 10.1081/Ncn-120023011  0.833
2003 Johansson T, Stawinski J. Studies towards synthesis of dinucleoside arylphosphonates with metal complexing properties. Nucleosides, Nucleotides & Nucleic Acids. 22: 1459-61. PMID 14565442 DOI: 10.1081/Ncn-120023010  0.789
2003 Bollmark M, Johansson T, Kullberg M, Nilsson J, Stawinski J, Cieslak J, Jankowska J, Sobkowski M, Szymczak M, Wenska M, Kraszewski A. Developing synthetic methods for bioactive phosphorus compounds using H-phosphonate chemistry: a progress report. Nucleosides, Nucleotides & Nucleic Acids. 22: 617-21. PMID 14565239 DOI: 10.1081/NCN-120021966  0.826
2003 Szymczak M, Szymańska A, Stawiński J, Boryski J, Kraszewski A. Aryl h-phosphonates. 14. Synthesis of new nucleotide analogues with phosphonate-phosphate internucleosidic linkage. Organic Letters. 5: 3571-3. PMID 14507175 DOI: 10.1021/Ol035166U  0.842
2003 Zmudzka K, Johansson T, Wojcik M, Janicka M, Nowak M, Stawinski J, Nawrot B. Novel DNA analogues with 2-, 3- and 4-pyridylphosphonate internucleotide bonds: synthesis and hybridization properties New Journal of Chemistry. 27: 1698. DOI: 10.1039/B305689A  0.766
2002 Stawinski J, Kraszewski A. How to get the most out of two phosphorus chemistries. Studies on H-phosphonates. Accounts of Chemical Research. 35: 952-60. PMID 12437320 DOI: 10.1021/Ar010049P  0.804
2002 Gołos B, Dzik JM, Kazimierczuk Z, Cieśla J, Zieliński Z, Jankowska J, Kraszewski A, Stawiński 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. 382: 1439-45. PMID 11727827 DOI: 10.1515/Bc.2001.177  0.782
2002 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. 9: 2315-22. PMID 11553470 DOI: 10.1016/S0968-0896(01)00140-7  0.847
2002 Kullberg M, Bollmark M, Stawinski J. Triphenyl phosphoroselenoate – a new selenizing agent for P(III) compounds Collection of Czechoslovak Chemical Communications. 5: 290-294. DOI: 10.1135/Css200205290  0.829
2002 Sobkowski M, Cieślak J, Jankowska J, Stawinski J, Kraszewski A. Dinucleoside aryl phosphorothioates as building blocks for large scale synthesis of chimeric oligonucleotide analogues Collection of Czechoslovak Chemical Communications. 5: 283-289. DOI: 10.1135/Css200205283  0.788
2002 Stawinski J, Kraszewski A. H-Phosphonates – chemistry and applications Collection of Czechoslovak Chemical Communications. 5: 272-282. DOI: 10.1135/Css200205272  0.806
2002 Nilsson J, Stawinski J. Oxidative coupling of H-phosphonate and H-phosphonothioate diesters. Iodine as a reagent and a catalyst Collection of Czechoslovak Chemical Communications. 5: 87-92. DOI: 10.1135/Css200205087  0.703
2002 Johansson T, Stawinski J. Studies on the synthesis of picolylphosphonate diesters Collection of Czechoslovak Chemical Communications. 5: 81-86. DOI: 10.1135/Css200205081  0.797
2002 Johansson T, Stawinski J. Synthesis of Nucleotide Analogues with Pyridylphosphonate and Pyridylphosphono thio ate Internucleotide Linkages Phosphorus, Sulfur, and Silicon and the Related Elements. 177: 1779-1782. DOI: 10.1080/10426500212320  0.804
2002 Nilsson J, Bollmark M, Jankowska J, Wenska M, Cieslak J, Kraszewski A, Stawinski J. New Synthetic Methods for Nucleotide Analogues Based on H-Phosphonate Chemistry: A Progress Report Phosphorus, Sulfur, and Silicon and the Related Elements. 177: 1513-1516. DOI: 10.1080/10426500212261  0.851
2002 Cieślak J, Jankowska J, Sobkowski M, Wenska M, Stawiński J, Kraszewski A. Aryl H-phosphonates. Part 13. A new, general entry to aryl nucleoside phosphate and aryl nucleoside phosphorothioate diesters Journal of the Chemical Society-Perkin Transactions 1. 31-37. DOI: 10.1039/B109373H  0.865
2002 Stamatov SD, Stawinski J. Novel, regioselective transformation of an oxirane system. An efficient approach to the synthesis of endocannabinoid 2-arachidonoylglycerol Tetrahedron Letters. 43: 1759-1761. DOI: 10.1016/S0040-4039(02)00116-8  0.432
2002 Bollmark M, Kullberg M, Stawinski J. Nucleoside H-phosphonates. Part 19: Novel nucleotide analogues—H-phosphonoselenoate mono- and diesters Tetrahedron Letters. 43: 515-518. DOI: 10.1016/S0040-4039(01)02182-7  0.859
2001 Stawinski J, Strömberg R. Deoxyribo- and ribonucleoside H-phosphonates. Current Protocols in Nucleic Acid Chemistry. Unit 2.6. PMID 18428839 DOI: 10.1002/0471142700.Nc0206S04  0.699
2001 Cieślak J, Sobkowski M, Jankowska J, Wenska M, Szymczak M, Imiolczyk B, Zagórowska I, Shugar D, Stawiński J, Kraszewski A. Nucleoside phosphate analogues of biological interest, and their synthesis via aryl nucleoside H-phosphonates as intermediates. Acta Biochimica Polonica. 48: 429-442. DOI: 10.18388/Abp.2001_3927  0.858
2001 Johansson T, Stawinski J. Synthesis of dinucleoside pyridylphosphonates involving palladium(0)-catalysed phosphorus–carbon bond formation as a key step Chemical Communications. 2564-2565. DOI: 10.1039/B108857M  0.797
2001 Nilsson J, Kraszewski A, Stawinski J. Reinvestigation of the 31P NMR evidence for the formation of diorganyl phosphoropyridinium intermediates Journal of the Chemical Society-Perkin Transactions 1. 2263-2266. DOI: 10.1039/B107792A  0.8
2001 Bollmark M, Stawinski J. A new selenium-transferringreagent—triphenylphosphine selenide Chemical Communications. 771-772. DOI: 10.1039/B101002F  0.766
2001 Wenska M, Jankowska J, Sobkowski M, Stawiński J, Kraszewski A. A new method for the synthesis of nucleoside 2′,3′-O,O-cyclic phosphorodithioates via aryl cyclic phosphites as intermediates Tetrahedron Letters. 42: 8055-8058. DOI: 10.1016/S0040-4039(01)01695-1  0.796
2001 Johansson T, Kers A, Stawinski J. 2-Pyridylphosphonates: a new type of modification for nucleotide analogues Tetrahedron Letters. 42: 2217-2220. DOI: 10.1016/S0040-4039(01)00115-0  0.822
2001 Stamatov SD, Stawinski J. ChemInform Abstract: A Simple and Efficient Method for Direct Acylation of Acetals with Long Alkyl-Chain Carboxylic Acid Anhydrides. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200114085  0.309
2000 Sobkowski M, Wenska M, Kraszewski A, Stawiński J. Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part VI. Reaction with diols. Nucleosides, Nucleotides & Nucleic Acids. 19: 1487-503. PMID 11200254 DOI: 10.1080/15257770008045441  0.845
2000 Cieślak J, Jankowska J, Stawiński 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. 65: 7049-54. PMID 11031027 DOI: 10.1021/Jo000729Q  0.834
2000 Jankowska J, Wenska M, Popenda M, Stawiński J, Kraszewski A. A new, efficient entry to nucleoside 2′,3′-O,O-cyclophosphorothioates Tetrahedron Letters. 41: 2227-2229. DOI: 10.1016/S0040-4039(00)00132-5  0.788
2000 Stamatov SD, Stawinski J. A Simple and Efficient Method for Direct Acylation of Acetals with Long Alkyl-Chain Carboxylic Acid Anhydrides Tetrahedron. 56: 9697-9703. DOI: 10.1016/S0040-4020(00)00924-8  0.448
1999 Kers I, Stawiński J, Girardet JL, Imbach JL, Périgaud C, Gosselin G, Aubertin AM. Synthesis and anti-retroviral activity of O,O'-bis(3'-azido-2',3'-dideoxythymidin-5'-yl) phosphoramidate derivatives. Nucleosides & Nucleotides. 18: 2317-25. PMID 10616733 DOI: 10.1080/07328319908044884  0.789
1999 Kers I, Girardet JL, Gosselin G, Perigaud C, Imbach JL, Stawinski J. Synthesis and in vitro antiviral activity of some symmetrical phosphoramidate dimers of AZT. Nucleosides & Nucleotides. 18: 993-4. PMID 10432728 DOI: 10.1080/15257779908041626  0.439
1999 Johansson T, Bollmark M, Stawinski J. Studies on sulfurisation of H-phosphonate diesters in the presence of diazabicyclo[5.4.0]undec-7-ene (DBU) Collection of Czechoslovak Chemical Communications. 2: 75-78. DOI: 10.1135/Css199902075  0.848
1999 Kers A, Kers I, Stawinski J, Cieślak J, Jankowska J, Kraszewski A. Developing synthetic methods for nucleotide analogues. A progress report Collection of Czechoslovak Chemical Communications. 2: 69-74. DOI: 10.1135/Css199902069  0.787
1999 Cieślak J, Jankowska J, Sobkowski M, Kers A, Kers I, Stawinski J, Kraszewski A. The reactions of aryl nucleoside H-phosphonates with O-, N-, and S-nucleophiles Collection of Czechoslovak Chemical Communications. 2: 63-68. DOI: 10.1135/Css199902063  0.822
1999 Kers A, Kers I, Cieslak J, Kraszewski A, Stawinski J. 31P NMR Studies on Oxidative Transformations of Aryl Nucleoside H-Phosphonate Diesters Nucleosides and Nucleotides. 18: 991-992. DOI: 10.1080/15257779908041625  0.849
1999 Cieślak J, Jankowska J, Szymczak M, Kers A, Kers I, Stawiński J, Kraszewski A. Aryl Nucleoside H-Phosphonates—Novel Derivatives of Controlled Reactivity Nucleosides and Nucleotides. 18: 937-938. DOI: 10.1080/15257779908041603  0.858
1999 Kers I, Bollmark M, Kraszewski A, Stawinski J. New Methods for the Formation of the P-N and P-F Bonds, their Relevance to Nucleotide and Oligonucleotide Analogues Synthesis Phosphorus, Sulfur, and Silicon and the Related Elements. 144: 637-640. DOI: 10.1080/10426509908546325  0.83
1999 Kers I, Kraszewski A, Stawinski J. Nucleoside Phosphoramidate Analogues with Modification in the Bridging Positions of the Phosphodiester Linkage Phosphorus, Sulfur, and Silicon and the Related Elements. 147: 169-169. DOI: 10.1080/10426509908053565  0.855
1999 Kers A, Stawinski J. Reaction of H-Phosphonate Diesters with Trityl Halides Phosphorus, Sulfur, and Silicon and the Related Elements. 147: 167-167. DOI: 10.1080/10426509908053564  0.82
1999 Kers I, Cieslak J, Jankowska J, Kraszewski A, Stawinski J. New Methods for Multiple Modifications of a Phosphorus Centre. Their Relevance to Nucleotide and Oligonucleotide Analogues Synthesis Nucleosides and Nucleotides. 18: 1245-1246. DOI: 10.1080/07328319908044678  0.817
1999 Bollmark M, Stawinski J. A Mild Method for the Preparation of Nucleoside Phosphorofluoridate and Phosphorofluoridothioate Diesters Nucleosides and Nucleotides. 18: 1243-1244. DOI: 10.1080/07328319908044677  0.766
1999 Cieslak J, Szymczak M, Wenska M, Stawinski J, Kraszewski A. Aryl H-phosphonates. Part 11. Synthetic and 31P NMR studies on the formation of aryl nucleoside H-phosphonates† Journal of the Chemical Society-Perkin Transactions 1. 3327-3331. DOI: 10.1039/A907150D  0.842
1999 Misiura K, Stec WJ, Bollmark M, Stawinski J. Studies on enzymatic hydrolysis of thymidin-3′-yl thymidin-5′-yl phosphorofluoridates and the corresponding phosphorothiofluoridates Chemical Communications. 2115-2116. DOI: 10.1039/A906659D  0.728
1999 Kers A, Szabó T, Stawinski J. Preparation of nucleoside 5′-deoxy-5′-methylenephosphonates as building blocks for the synthesis of methylenephosphonate analogues Journal of the Chemical Society-Perkin Transactions 1. 2585-2590. DOI: 10.1039/A906066I  0.815
1999 Kers A, Kers I, Stawinski J. 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 Journal of the Chemical Society-Perkin Transactions 1. 2071-2075. DOI: 10.1039/A904502C  0.808
1999 Kers A, Stawiński J. A new type of nucleotide analogue with 4-pyridylphosphonate internucleotide linkage Tetrahedron Letters. 40: 4263-4266. DOI: 10.1016/S0040-4039(99)00702-9  0.819
1999 Kers I, Kers A, Stawiński J, Kraszewski A. Aryl Hphosphonates. 8. Simple and efficient method forv the preparation of nucleoside Hphosphonothioate monoesters Tetrahedron Letters. 40: 3945-3948. DOI: 10.1016/S0040-4039(99)00617-6  0.852
1999 Kers I, Stawiński J, Kraszewski A. Aryl H-phosphonates. 10. Synthesis of nucleoside phosphoramidate and nucleoside phosphoramidothioate analogues via H-phosphonamidate intermediates Tetrahedron. 55: 11579-11588. DOI: 10.1016/S0040-4020(99)00656-0  0.872
1999 Kers A, Dembkowski L, Kraszewski A, Stawinski J. Studies on the reaction of trityl derivatives withH-phosphonate diesters: Their relevance to the synthesis of 4-pyridylphosphonates Heteroatom Chemistry. 10: 492-499. DOI: 10.1002/(Sici)1098-1071(1999)10:6<492::Aid-Hc10>3.0.Co;2-D  0.859
1998 Sobkowski M, Kraszewski A, Stawiński 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. 17: 253-67. PMID 9708350 DOI: 10.1080/07328319808005174  0.821
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. 15: 987-98. PMID 9619519 DOI: 10.1080/07391102.1998.10508218  0.342
1998 Kers A, Kers I, Bollmark M, Stawinski J. A Cautionary Note on the Use of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) in Conjunction with Chlorophosphates. Acta Chemica Scandinavica. 52: 1405-1406. DOI: 10.3891/Acta.Chem.Scand.52-1405  0.752
1998 Sandnes RW, Gacek M, Undheim K, Stawinski J. A Simple Synthesis of the Macrocycle 1,4,7,10-Tetraazacyclododecane. Acta Chemica Scandinavica. 52: 1402-1404. DOI: 10.3891/Acta.Chem.Scand.52-1402  0.466
1998 Bruno M, Herstad O, Holm JL, Stawinski J. Stability and Structure of Sodium Tetrafluoroaluminate, NaAlF4. Acta Chemica Scandinavica. 52: 1399-1401. DOI: 10.3891/Acta.Chem.Scand.52-1399  0.316
1998 Sydnes LK, Mungaroo R, Svendsen JS, Stawinski J. Silver Ion-assisted Solvolysis of 2,2-Dibromo-1-phenylcyclopropanecarboxylic Acid: Solvent-dependent Competition between Decarboxylation and Ring Closure. Acta Chemica Scandinavica. 52: 1392-1398. DOI: 10.3891/Acta.Chem.Scand.52-1392  0.358
1998 Sydnes LK, Mungaroo R, Aanesen BA, Stawinski J. Silver Ion-assisted Solvolysis of trans-2,2-Dibromo-1,3-dimethylcyclopropanecarboxylic Acid: Selective Formation of 4-Bromo-3,5-dimethyl-2(5H)-furanone. Acta Chemica Scandinavica. 52: 1386-1391. DOI: 10.3891/Acta.Chem.Scand.52-1386  0.473
1998 Kulińska K, Kuliński T, Stawiński J. Hydration of C-H groups in natural dithymidine nucleotide and its methylphosphonate analogues. Acta Biochimica Polonica. 45: 977-985. DOI: 10.18388/Abp.1998_4355  0.474
1998 Stawiński J, Kraszewski A. Some aspects of oligoribonucleotides synthesis via the H-phosphonate approach. Acta Biochimica Polonica. 45: 907-915. DOI: 10.18388/Abp.1998_4349  0.829
1998 Bollmark M, Stawinski J. Nucleotide Analogues Containing the P-F Bond. An Overview of the Synthetic Methods Nucleosides, Nucleotides and Nucleic Acids. 17: 663-680. DOI: 10.1080/07328319808005208  0.736
1998 Jankowska J, Sobkowska A, Cieślak J, Sobkowski M, Kraszewski A, Stawiński J, Shugar D. NucleosideH-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 The Journal of Organic Chemistry. 63: 8150-8156. DOI: 10.1021/Jo980491U  0.836
1998 Kers I, Stawiński J, Kraszewski A. A new synthetic method for the preparation of nucleoside phosphoramidate analogues with the nitrogen atom in bridging positions of the phosphoramidate linkage Tetrahedron Letters. 39: 1219-1222. DOI: 10.1016/S0040-4039(97)10734-1  0.866
1997 Kulinska K, Sarzyńska J, Szabo T, Stawiński 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. 15: 119-28. PMID 9283985 DOI: 10.1080/07391102.1997.10508951  0.754
1997 Zain R, Bollmark M, Stawinski J. Studies on Nucleoside H-Phosphonothioates as Synthons in the Synthesis of Oligonucleotide Analogues Nucleosides and Nucleotides. 16: 1661-1662. DOI: 10.1080/07328319708006250  0.861
1997 Bollmark M, Kers A, Kers I, Szabó T, Zain R, Stawiński J, Cieślak J, Jankowska J, Kraszewski A. Studies on Nucleoside Phosphonates and Their Derivatives. a Progress Report Nucleosides and Nucleotides. 16: 679-684. DOI: 10.1080/07328319708002934  0.789
1997 Bollmark M, Stawinski J. A new method for the formation of the P–F bond Chemical Communications. 991-992. DOI: 10.1039/A701728F  0.75
1997 Sobkowska A, Sobkowski M, Cieślak J, Kraszewski A, Kers I, Stawiński J. ArylH-Phosphonates. 6. Synthetic Studies on the Preparation of NucleosideN-Alkyl-H-phosphonamidates The Journal of Organic Chemistry. 62: 4791-4794. DOI: 10.1021/Jo962224Z  0.87
1997 Jankowska J, Cieślak J, Kraszewski A, Stawiński J. 9-Fluorenemethyl H-phosphonothioate, a versatile reagent for the preparation of H-phosphonothioate, phosphorothioate, and phosphorodithioate monoesters Tetrahedron Letters. 38: 2007-2010. DOI: 10.1016/S0040-4039(97)00218-9  0.837
1997 Kers A, Stawiński J, Dembkowski L, Kraszewski A. 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. DOI: 10.1016/S0040-4020(97)00790-4  0.857
1996 Zain R, Stawinski J. Nucleoside H-Phosphonates. 17. Synthetic and (31)P NMR Studies on the Preparation of Dinucleoside H-Phosphonothioates. The Journal of Organic Chemistry. 61: 6617-6622. PMID 11667530 DOI: 10.1021/Jo960810M  0.793
1996 Almer H, Stawinski J, Strömberg R. Solid support synthesis of all-Rp-oligo(ribonucleoside phosphorothioate)s. Nucleic Acids Research. 24: 3811-20. PMID 8871563 DOI: 10.1093/Nar/24.19.3811  0.706
1996 Kers A, Kers I, Kraszewski A, Stawinski J. 31P NMR studies on the activation pathways of aryl H-phosphonate esters with condensing agents Collection of Czechoslovak Chemical Communications. 61: 246-249. DOI: 10.1135/Cccc1996S246  0.834
1996 Cieslak J, Jankowska J, Kers A, Kers I, Sobkowska A, Sobkowski M, Stawinski J, Kraszewski A. Synthetic applications of aryl H-phosphonates in nucleotide chemistry Collection of Czechoslovak Chemical Communications. 61: 242-245. DOI: 10.1135/Cccc1996S242  0.847
1996 Sobkowski M, Stawinski J, Kraszewski A. 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 Collection of Czechoslovak Chemical Communications. 61: 238-241. DOI: 10.1135/Cccc1996S238  0.851
1996 Bollmark M, Zain R, Stawinski J. Efficient method for the preparation of nucleoside phosphorofluoridates and nucleoside phosphorofluoridothioates Collection of Czechoslovak Chemical Communications. 61: 68-71. DOI: 10.1135/Cccc1996S068  0.793
1996 Stawiński J, Kraszewski A, Sobkowski M. Exploring Reactions of Nucleoside H-Phosphonates with Bifunctional Reagents Phosphorus Sulfur and Silicon and the Related Elements. 109: 261-264. DOI: 10.1080/10426509608545140  0.838
1996 Kers A, Kers I, Kraszewski A, Sobkowski M, Szabó T, Thelin M, Zain R, Stawinski J. Nucleoside Phosphonates. Development of Synthetic Methods and Reagents Nucleosides and Nucleotides. 15: 361-378. DOI: 10.1080/07328319608002390  0.788
1996 Zain R, Stawiński J. Nucleoside H-phosphonates. Part 16. 31P NMR studies on the transformation of nucleoside H-phosphonate monoesters into a monofunctional tervalent intermediate, nucleoside acyl silyl phosphite Journal of the Chemical Society-Perkin Transactions 1. 795-799. DOI: 10.1039/P29960000795  0.792
1996 Bollmark M, Stawiński J. A facile access to nucleoside phosphorofluoridate, nucleoside phosphorofluoridothioate, and nucleoside phosphorofluoridodithioate monoesters Tetrahedron Letters. 37: 5739-5742. DOI: 10.1016/0040-4039(96)01171-9  0.817
1996 Cieślak J, Sobkowski M, Kraszewski A, Stawiński J. Aryl H-phosphonates. Part IV. A new method for internucleotide bond formation based on transesterification of aryl nucleoside H-phosphonate diesters Tetrahedron Letters. 37: 4561-4564. DOI: 10.1016/0040-4039(96)00846-5  0.867
1996 Bollmark M, Zain R, Stawiński J. A new entry to nucleoside phosphorofluoridate and nucleoside phosphorofluoridothioate diesters Tetrahedron Letters. 37: 3537-3540. DOI: 10.1016/0040-4039(96)00606-5  0.854
1996 Kers A, Kers I, Stawiński J, Sobkowski M, Kraszewski A. Studies on aryl H-phosphonates. 3. Mechanistic investigations related to the disproportionation of diphenyl H-phosphonate under anhydrous basic conditions Tetrahedron. 52: 9931-9944. DOI: 10.1016/0040-4020(96)00525-X  0.861
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. 23: 893-900. PMID 7731801 DOI: 10.1093/Nar/23.6.893  0.808
1995 Szabó T, Stawinski J, Carlson S, Norrestam R. The SP Diastereomer of a Dinucleoside Methylphosphonate Methanol Solvate Containing Thymine and N3-Methyl-4-thiothymine Bases Acta Crystallographica Section C Crystal Structure Communications. 51: 411-415. DOI: 10.1107/S0108270194006281  0.244
1995 Westman E, Sigurdsson S, Almer H, Thelin M, Stawinski J, Rozners E, Strömbetg R. Rna-synthesis using the h-phosphonate approach and an improved protecting group strategy Nucleosides and Nucleotides. 14: 883-887. DOI: 10.1080/15257779508012495  0.804
1995 Almer H, Stawinski J, Strömberg R. Chemical Synthesis of RNA-Fragment Analogues That Have Phosphorothioate Linkages of Identical Configuration Nucleosides, Nucleotides and Nucleic Acids. 14: 879-881. DOI: 10.1080/15257779508012494  0.695
1995 Szabó T, Kers A, Stawinski J. Solid Phase Synthesis of 5'-Methylenephosphonate DNA Nucleosides, Nucleotides and Nucleic Acids. 14: 871-874. DOI: 10.1080/15257779508012492  0.762
1995 Szabóa T, Almer H, Ströumberg R, Stawinski J. 2-Cyanoethyl H-Phosphonate. A Reagent for the Mild Preparation of Nucleoside H-Phosphonate Monoesters Nucleosides, Nucleotides and Nucleic Acids. 14: 715-716. DOI: 10.1080/15257779508012456  0.614
1995 Stawinski J, Zain R. Conversion of Nucleoside H-Phosphonate Monoesters to the Corresponding H-Phosphonothioates. 31P NMR Studies Nucleosides, Nucleotides and Nucleic Acids. 14: 711-714. DOI: 10.1080/15257779508012455  0.793
1995 Kers A, Kers I, Stawiński J, Sobkowski M, Kraszewski A. Studies on Aryl H-Phosphonates; Part 2: A General Method for the Preparation of Alkyl H-Phosphonate Monoesters Synthesis. 1995: 427-430. DOI: 10.1055/S-1995-3919  0.853
1995 Zain R, Stroemberg R, Stawinski J. Nucleoside H-Phosphonates. 15. Preparation of Nucleoside H-Phosphonothioate Monoesters from the Corresponding Nucleoside H-Phosphonates The Journal of Organic Chemistry. 60: 8241-8244. DOI: 10.1021/Jo00130A025  0.781
1995 Sobkowski M, Stawiński J, Kraszewski A. Studies on reactions of nucleoside H-phosphonate diesters 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 Letters. 36: 2295-2298. DOI: 10.1016/0040-4039(95)00238-8  0.828
1995 Szabó T, Stawiński J. 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 [p(ch2Tp(ch2T] Tetrahedron. 51: 4145-4160. DOI: 10.1016/0040-4020(95)00131-Q  0.775
1994 Gosselin G, Périgaud C, Lefebvre I, Pompon A, Aubertin AM, Kirn A, Szabo T, Stawinski J, Imbach JL. 5'-Hydrogenphosphonates of anti-HIV nucleoside analogues revisited: controversial mode of action. Antiviral Research. 22: 143-53. PMID 8279809 DOI: 10.1016/0166-3542(93)90092-W  0.767
1994 Sobkowski M, Stawiński J, Sobkowska A, Kraszewski A. Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part 2. Stability of nucleoside H-phosphonate diesters in the presence of amino alcohols Journal of the Chemical Society-Perkin Transactions 1. 1803-1808. DOI: 10.1039/P19940001803  0.828
1994 Almer H, Stawinski J, Strömberg R. Synthesis of stereochemically homogeneous oligoribonucleoside all-Rp-phosphorothioates by combining H-phosphonate chemistry and enzymatic digestion Journal of the Chemical Society, Chemical Communications. 1459-1460. DOI: 10.1039/C39940001459  0.729
1994 Clivio P, Fourrey J, Szabo T, Stawinski J. Photochemistry of Di(deoxyribonucleoside) Methylphosphonates Containing N3-Methyl-4-thiothymine The Journal of Organic Chemistry. 59: 7273-7283. DOI: 10.1021/Jo00103A018  0.741
1994 Stawinski J, Thelin M. 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 The Journal of Organic Chemistry. 59: 130-136. DOI: 10.1021/Jo00080A021  0.849
1994 Jankowska J, Sobkowski M, Stawiński J, Kraszewski A. Studies on aryl H-phosphonates. I. An efficient method for the preparation of deoxyribo- and ribonucleoside 3′-H-phosphonate monoesters by transesterification of diphenyl H-phosphonate Tetrahedron Letters. 35: 3355-3358. DOI: 10.1016/S0040-4039(00)76906-1  0.86
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. 21: 3921-6. PMID 8371969 DOI: 10.1093/Nar/21.17.3921  0.751
1993 Westman E, Stawinski J, Strömberg R. RNA-synthesis using H-phosphonates. Synchronizing 2'-OH and N-protection Collection of Czechoslovak Chemical Communications. 58: 236-237. DOI: 10.1135/Cccc1993S236  0.823
1993 Almer H, Westman E, Rozners E, Stawinski J, Strömberg R. Advances in synthesis of oligoribonucleotides and their phosphorothioate analogues using the H-phosphonate approach Collection of Czechoslovak Chemical Communications. 58: 82. DOI: 10.1135/Cccc1993S082  0.847
1993 Stawinski J, Strömberg R, Zain R. Hydrolytic stability of nucleoside H-phosphonate and H-phosphonothioate diesters Collection of Czechoslovak Chemical Communications. 58: 79-81. DOI: 10.1135/Cccc1993S079  0.817
1993 Kraszewski A, Sobkowskia M, Stawiński J. Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part 1. Reaction with amino alcohols Journal of the Chemical Society-Perkin Transactions 1. 1699-1704. DOI: 10.1039/P19930001699  0.803
1992 Almer H, Stawinski J, Stroemberg R, Thelin M. Synthesis of diribonucleoside phosphorothioates via stereospecific sulfuration of H-phosphonate diesters The Journal of Organic Chemistry. 57: 6163-6169. DOI: 10.1021/Jo00049A022  0.848
1992 Stawiński J, Thelin M. 3-H-2,1-benzoxathiol-3-one 1-oxide - a new reagent for stereospecific oxidation of nucleoside H-phosphonothioate diesters Tetrahedron Letters. 33: 3189-3192. DOI: 10.1016/S0040-4039(00)79848-0  0.831
1992 Stawiński J, Strömberg R, Zain R. Stereospecific oxidation and oxidative coupling of H-phosphonate and H-phosphonothioate diesters Tetrahedron Letters. 33: 3185-3188. DOI: 10.1016/S0040-4039(00)79847-9  0.812
1992 Stawiński J, Thelin M. 3H-1,2-benzothiaselenol-3-one. A new selenizing reagent for nucleoside H-phosphonate and H-phosphonothioate diesters Tetrahedron Letters. 33: 7255-7258. DOI: 10.1016/S0040-4039(00)60887-0  0.841
1991 KOZAK E, STAWIŃSKI J, WIERZCHOŚ J. RELIABILITY OF MERCURY INTRUSION POROSIMETRY RESULTS FOR SOILS Soil Science. 152: 405-413. DOI: 10.1097/00010694-199112000-00002  0.165
1991 Stawinski J, Strömberg R, Westman E. Ribonucleoside H-Phosphonates. Pyridine vs Quinoline - Influence on Condensation Rate Nucleosides and Nucleotides. 10: 519-520. DOI: 10.1080/07328319108046514  0.817
1991 Stawinski J, Thelin M, Von Stedingk E. Studies on Sulfurization of Nucleoside H-Phosphonate and H-Phosphonothioate Esters Using 3H-1,2-Benzodithiol.3-one 1,1-dioxide Nucleosides and Nucleotides. 10: 517-518. DOI: 10.1080/07328319108046513  0.835
1991 Stawinski J, Stromberg R, Zain R. Studies on the Conversion of Nucleoside H-Phosphonate Monoesters into the Corresponding H-Phosphonothioates Nucleosides and Nucleotides. 10: 515-516. DOI: 10.1080/07328319108046512  0.833
1991 Stawinski J, Stromberg R, Thelin M. Some Chemical and Stereochemical Aspects of Ribonucleoside H-Phosphonate and H-Phosphonothioate Diester Synthesis Nucleosides and Nucleotides. 10: 511-514. DOI: 10.1080/07328319108046511  0.858
1991 Stawinski J, Thelin M. Nucleoside H-phosphonates. 13. Studies on 3H-1,2-benzodithiol-3-one derivatives as sulfurizing reagents for H-phosphonate and H-phosphonothioate diesters The Journal of Organic Chemistry. 56: 5169-5175. DOI: 10.1021/Jo00017A033  0.838
1990 Stawinski J, Strömberg R, Szabó T. Synthesis of nucleoside methylphosphonates and nucleoside methylthiophosphonates via phosphinate intermediates Collection of Czechoslovak Chemical Communications. 55: 145-148. DOI: 10.1135/Cccc1990S145  0.818
1990 Stawinski J, Szabó T, Thelin M, Westman E, Zain R. Studies on the preparation of nucleoside H-phosphonothioates Collection of Czechoslovak Chemical Communications. 55: 141-144. DOI: 10.1135/Cccc1990S141  0.847
1990 Stawinski J, Thelin M. Nucleoside H-Phosphonates. XI. A Convenient Method for the Preparation of Nucleoside H-Phosphonates Nucleosides and Nucleotides. 9: 129-135. DOI: 10.1080/07328319008045116  0.855
1990 Stawinski J, Thelin M. Studies on the activation pathway of phosphonic acid using acyl chlorides as activators Journal of the Chemical Society-Perkin Transactions 1. 849-853. DOI: 10.1039/P29900000849  0.812
1990 Stawinski J, Thelin M, Westman E, Zain R. Nucleoside H-phosphonates. 12. Synthesis of nucleoside 3'-(hydrogen phosphonothioate) monoesters via phosphinate intermediates The Journal of Organic Chemistry. 55: 3503-3506. DOI: 10.1021/Jo00298A023  0.841
1990 STAWINSKI J, THELIN M, WESTMAN E, ZAIN R. ChemInform Abstract: Nucleoside H-Phosphonates. Part 12. Synthesis of Nucleoside 3′-(Hydrogen Phosphonothioate) Monoesters via Phosphinate Intermediates. Cheminform. 21. DOI: 10.1002/chin.199043282  0.765
1990 STAWINSKI J, STROMBERG R, LINDH I, REGBERG T, SZABO T, THELIN M, WESTMAN E, GAREGG PJ. ChemInform Abstract: The H-Phosphonate Method for Constructing Phosphodiester Linkages. A Progress Report Cheminform. 21. DOI: 10.1002/chin.199019341  0.838
1989 Stawinski J, Strömberg R, Szabó T, Westman E. Recent Studies in Nucleoside Phosphonate Chemistry Nucleosides, Nucleotides and Nucleic Acids. 8: 1029-1032. DOI: 10.1080/07328318908054269  0.844
1989 Stawinski J, Stromberg R, Lindh I, Regberg T, Szabo T, Thelin M, Westman E, Garegg PJ. The H-phosphonate method for constructing phosphodiester linkages. A progress report Nucleosides and Nucleotides. 8: 799-803. DOI: 10.1080/07328318908054218  0.83
1989 Lindh I, Stawinski J. A general method for the synthesis of glycerophospholipids and their analogs via H-phosphonate intermediates The Journal of Organic Chemistry. 54: 1338-1342. DOI: 10.1021/Jo00267A020  0.6
1989 Stawiński J, Thelin M, Zain R. Nucleoside H-phosphonates. X. Studies on nucleoside hydrogenphosphonothioate diester synthesis Tetrahedron Letters. 30: 2157-2160. DOI: 10.1016/S0040-4039(01)93737-2  0.853
1989 LINDH I, STAWINSKI J. ChemInform Abstract: A General Method for the Synthesis of Glycerophospholipids and Their Analogues via H-Phosphonate Intermediates. Cheminform. 20. DOI: 10.1002/chin.198935354  0.544
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. 16: 9285-98. PMID 3174451 DOI: 10.1093/Nar/16.19.9285  0.824
1988 Huss S, Gosselin G, Stawinski J, Stromberg R, Imbach J. Studies on Ribonucleoside Hydrogenphosphonates. Effect of a Vicinal Hydroxyl Function on the Stability of H-Phosphonate Diester Bond Nucleosides and Nucleotides. 7: 321-337. DOI: 10.1080/07328318808068713  0.727
1988 Regberg T, Stawinski J, Ströberg R. Nucleoside H-Phosphonates. IX. Possible Side-Reactions During Hydrogen Phosphonate Diester Formation Nucleosides and Nucleotides. 7: 23-35. DOI: 10.1080/07328318808068700  0.818
1988 Stawinski J, Sternberg R, Thelin M, Westman E. Evaluation of the Use of the t-Butyldimethylsilyl Group for 2′-Protection in RNA-Synthesis Via the H-Phosphonate Approach Nucleosides and Nucleotides. 7: 779-782. DOI: 10.1080/07328318808056329  0.81
1988 Stawinski J, Stromberg R, Thelin M, Westman E. Reactions of Nucleoside Hydrogenphosphonates with Diphenyl Chlorophosphate and Sterically Hindered Aromatic Acyl Chlorides Nucleosides and Nucleotides. 7: 601-604. DOI: 10.1080/07328318808056293  0.851
1988 Patrykiejew A, Sokolowski S, Stawinski J, Sokołowska Z. The adsorption of simple multiatomic molecules in slit-like micropores Journal of Colloid and Interface Science. 124: 371-374. DOI: 10.1016/0021-9797(88)90360-8  0.173
1987 Strömberg R, Stawinski J. Iodine and Iodine Catalysed Phosphorylation of Nucleosides by Phosphorodiester Derivatives Nucleosides and Nucleotides. 6: 815-820. DOI: 10.1080/15257778708073428  0.612
1987 Garegg PJ, Regberg T, Stawinski J, Strömberg R. Nucleoside H-phosphonates. V. the mechanism of hydrogenphosphonate diester formation using acyl chlorides as coupling agents in oligonucleotide synthesis by the hydrogenphosphonate approach Nucleosides and Nucleotides. 6: 655-662. DOI: 10.1080/07328318708069994  0.85
1987 Garegg PJ, Regberg T, Stawinski J, Strömberg R. Studies on the Oxidation of Nucleoside Hydrogenphosphonates Nucleosides and Nucleotides. 6: 429-432. DOI: 10.1080/07328318708056247  0.82
1987 Garegg PJ, Stawinski J, Strömberg R. Activation of Nucleoside Hydrogenphosphonates by Use of Aryl Sulfonyl Chlorides Nucleosides and Nucleotides. 6: 425-427. DOI: 10.1080/07328318708056246  0.721
1987 Garegg PJ, Regberg T, Stawinski J, Stromberg R. Studies on the Synthesis of Oligonucleotidesviathe Hydrogenphosphonate Approach Nucleosides and Nucleotides. 6: 283-286. DOI: 10.1080/07328318708056205  0.81
1987 Garegg PJ, Stawinski J, Strömberg R. Nucleoside hydrogenphosphonates. Part 6. Reaction of nucleoside hydrogenphosphonates with arenesulphonyl chlorides Journal of the Chemical Society-Perkin Transactions 1. 1209-1214. DOI: 10.1039/P29870001209  0.649
1987 Garegg PJ, Regberg T, Stawiński J, Strömberg R. A phosphorus nuclear magnetic resonance spectroscopic study of the conversion of hydroxy groups into iodo groups in carbohydrates using the iodine–triphenylphosphine–imidazole reagent Journal of the Chemical Society-Perkin Transactions 1. 271-274. DOI: 10.1039/P29870000271  0.799
1987 Garegg PJ, Regberg T, Stawinski J, Strömberg R. Nucleoside phosphonates: part 7. Studies on the oxidation of nucleoside phosphonate esters Journal of the Chemical Society-Perkin Transactions 1. 1269-1273. DOI: 10.1039/P19870001269  0.786
1987 Garegg PJ, Stawinski J, Stroemberg R. Nucleoside 3'-H-phosphonates. 8. Activation of hydrogen phosphonate monoesters by chlorophosphates and arenesulfonyl derivatives The Journal of Organic Chemistry. 52: 284-287. DOI: 10.1021/Jo00378A026  0.679
1987 GAREGG PJ, STAWINSKI J, STROEMBERG R. ChemInform Abstract: Nucleoside Hydrogenphosphonates. Part 6. Reaction of Nucleoside Hydrogenphosphonates with Arenesulfonyl Chlorides. Cheminform. 18. DOI: 10.1002/chin.198751355  0.588
1987 GAREGG PJ, REGBERG T, STAWINSKI J, STROEMBERG R. ChemInform Abstract: Nucleoside Phosphonates. Part 7. Oxidation of Nucleoside Phosphonate Esters. Cheminform. 18. DOI: 10.1002/chin.198739316  0.788
1987 GAREGG PJ, STAWINSKI J, STROEMBERG R. ChemInform Abstract: Nucleoside H-Phosphonates. Part 8. Activation of Hydrogen Phosphonate Monoesters by Chlorophosphates and Arenesulfonyl Derivatives. Cheminform. 18. DOI: 10.1002/chin.198732322  0.65
1987 GAREGG PJ, REGBERG T, STAWINSKI J, STROEMBERG R. ChemInform Abstract: 31P NMR Spectroscopic Study of the Conversion of Hydroxy Groups into Iodo Groups in Carbohydrates Using the Iodine-Triphenylphosphine-Imidazole Reagent. Cheminform. 18. DOI: 10.1002/chin.198728147  0.794
1987 GAREGG PJ, LINDH I, REGBERG T, STAWINSKI J, STROEMBERG R, HENRICHSON C. ChemInform Abstract: Nucleoside H-Phosphonates. Part 3. Chemical Synthesis of Oligodeoxyribonucleotides by the Hydrogenphosphonate Approach. Nucleoside H-Phosphonates. Part 4. Automated Solid Phase Synthesis of Oligoribonucleotides by the Hydrogenphosphon Cheminform. 18. DOI: 10.1002/chin.198705305  0.853
1986 Garegg PJ, Lindh I, Regberg T, Stawinski J, Strömberg R, Henrichson C. Nucleoside H-phosphonates. IV. Automated solid phase synthesis of oligoribonucleotides by the hydrogenphosphonate approach Tetrahedron Letters. 27: 4055-4058. DOI: 10.1016/S0040-4039(00)84909-6  0.83
1986 Garegg PJ, Lindh I, Regberg T, Stawinski J, Strömberg R, Henrichson C. Nucleoside H-phosphonates. III. Chemical synthesis of oligodeoxyribonucleotides by the hydrogenphosphonate approach Tetrahedron Letters. 27: 4051-4054. DOI: 10.1016/S0040-4039(00)84908-4  0.859
1986 Garegg PJ, Regberg T, Stawinski J, Strömberg R. Studies on the reaction of nucleoside phosphorodiesters with aryl sulfonyl chlorides Tetrahedron Letters. 27: 2665-2666. DOI: 10.1016/S0040-4039(00)84612-2  0.799
1986 GAREGG PJ, REGBERG T, STAWINSKI J, STROEMBERG R. ChemInform Abstract: Studies on the Reaction of Nucleoside Phosphorodiesters with Aryl Sulfonyl Chlorides. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198647364  0.809
1986 GAREGG PJ, REGBERG T, STAWINSKI J, STROEMBERG R. ChemInform Abstract: Nucleoside Hydrogenphosphonates in Oligonucleotide Synthesis. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198638311  0.814
1986 GAREGG PJ, REGBERG T, STAWINSKI J, STROEMBERG R. ChemInform Abstract: Formation of Internucleotidic Bonds via Phosphonate Intermediates. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198608300  0.781
1984 Narang SA, 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. 62: 209-16. PMID 6722637 DOI: 10.1139/o84-030  0.687
1984 Georges F, Brousseau R, Michniewicz J, Prefontaine G, Stawinski J, Sung W, Wu R, Narang SA. Synthesis of a human insulin gene. VII. Synthesis of preproinsulin-like human DNA, its cloning and expression in M13 bacteriophage. Gene. 27: 201-11. PMID 6373502 DOI: 10.1016/0378-1119(84)90141-0  0.707
1984 Jankowska J, Stawiński J. A Facile Synthesis of Cyclic of Phosphodiesters Synthesis. 1984: 408-410. DOI: 10.1055/S-1984-30855  0.46
1984 JANKOWSKA J, STAWINSKI J. ChemInform Abstract: A FACILE SYNTHESIS OF CYCLIC PHOSPHODIESTERS Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198442266  0.382
1983 STAWINSKI J, GRZESKOWIAK K, KRASZEWSKI A. ChemInform Abstract: p-Anisoyltetrazole: a New Anisoylating Reagent for Nucleosides. Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198346340  0.752
1980 Kraszewski A, Stawiński J, Wiewiórowski M. The case of sulfonation in the chemical synthesis of oligonucleotides. Nucleic Acids Research. 8: 2301-5. PMID 6253882 DOI: 10.1093/Nar/8.10.2301  0.811
1980 Kraszewski A, Stawiński J. Phosphoryl tris-triazole - a new phosphorylating reagent Tetrahedron Letters. 21: 2935-2936. DOI: 10.1016/S0040-4039(00)78649-7  0.743
1980 KRASZEWSKI A, STAWINSKI J. ChemInform Abstract: PHOSPHORYL TRIS-THIAZOLE - A NEW PHOSPHORYLATING REAGENT Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198042278  0.708
1978 Adamiak RW, Biała E, Grześkowiak K, Kierzek R, Kraszewski A, Markiewicz WT, Okupniak J, Stawiński 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. 5: 1889-905. PMID 673839 DOI: 10.1093/Nar/5.6.1889  0.795
1977 Adamiak RW, Biala E, Grześkowiak, Kierzek R, Kraszewski A, Markiewicz WT, Stawiński 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. 4: 2321-9. PMID 909778 DOI: 10.1093/Nar/4.7.2321  0.77
1977 Stawinski J, Hozumi T, Narang SA, Bahl CP, Wu R. Arylsulfonyltetrazoles, new coupling reagents and further improvements in the triester method for the synthesis of deoxyribooligonucleotides. Nucleic Acids Research. 4: 353-71. PMID 190591 DOI: 10.1093/Nar/4.2.353  0.752
1977 Adamiak RW, Stawiński J. A highly effective route to N,N′-disubstituted ureas under mild conditions. an application to the synthesis of tRNA anticodon loop fragments containing ureidonucleosides. Tetrahedron Letters. 18: 1935-1936. DOI: 10.1016/S0040-4039(01)83645-5  0.416
1977 ADAMIAK RW, STAWINSKI J. ChemInform Abstract: A HIGHLY EFFECTIVE ROUTE TO N,N′-DISUBSTITUTED UREAS UNDER MILD CONDITIONS. AN APPLICATION TO THE SYNTHESIS OF TRNA ANTICODON LOOP FRAGMENTS CONTAININ UREIDONUCLEOSIDES Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/chin.197739370  0.328
1976 Marians KJ, Wu R, Stawinski J, Hozumi T, Narang SA. Cloned synthetic lac operator DNA is biologically active Nature. 263: 744-748. PMID 792711 DOI: 10.1038/263744A0  0.702
1976 Stawinski J, Hozumi T, Narang SA. Benzoyltetrazole: a mild benzoylating reagent for nucleosides Journal of the Chemical Society, Chemical Communications. 243-244. DOI: 10.1039/C39760000243  0.724
1976 STAWINSKI J, HOZUMI T, NARANG SA. ChemInform Abstract: BENZOYLTETRAZOLE- A MILD BENZOYLATING REAGENT FOR NUCLEOSIDES Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/Chin.197631238  0.76
1976 Stawinski J, Hozumi T, Narang SA. Arylsulfonyltetrazoles as highly efficient condensing reagents for polynucleotide synthesis Canadian Journal of Chemistry. 54: 670-672. DOI: 10.1002/Chin.197627345  0.769
1976 STAWINSKI J, HOZUMI T, NARANG SA. ChemInform Abstract: ARYLSULFONYLTETRAZOLES AS HIGHLY EFFICIENT CONDENSING REAGENTS FOR POLYNUCLEOTIDE SYNTHESIS Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/chin.197627345  0.749
1975 GRZESKOWIAK K, STAWINSKI J, WIEWIOROWSKI M. ChemInform Abstract: A NEW EXAMPLE OF THE PROTECTED TRIESTER NUCLEOTIDE AS A KEY INTERMEDIATE FOR SYNTHESIS OF OLIGORIBONUCLEOTIDES Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197547431  0.476
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