| Year |
Citation |
Score |
| 2024 |
Rojewska M, Romanowska J, Kraszewski A, Sobkowski M, Prochaska K. The Interactions of Anti-HIV Pronucleotides with a Model Phospholipid Membrane. Molecules (Basel, Switzerland). 29. PMID 39683946 DOI: 10.3390/molecules29235787 |
0.782 |
|
| 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 |
0.803 |
|
| 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 |
0.814 |
|
| 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 |
0.634 |
|
| 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 |
0.609 |
|
| 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 |
0.686 |
|
| 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 |
0.795 |
|
| 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 |
0.774 |
|
| 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 |
0.766 |
|
| 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 |
0.832 |
|
| 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 |
0.86 |
|
| 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 |
0.77 |
|
| 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 |
0.827 |
|
| 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 |
0.823 |
|
| 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 |
0.847 |
|
| 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 |
0.857 |
|
| 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 |
0.685 |
|
| 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 |
0.856 |
|
| 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 |
0.831 |
|
| 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 |
0.86 |
|
| 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 |
0.722 |
|
| 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 |
0.614 |
|
| 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 |
0.828 |
|
| 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 |
0.807 |
|
| 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 |
0.85 |
|
| 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 |
0.843 |
|
| 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 |
0.819 |
|
| 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 |
0.778 |
|
| 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 |
0.762 |
|
| 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 |
0.824 |
|
| 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 |
0.802 |
|
| 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 |
0.809 |
|
| 2006 |
Sierosławski K, Slepokura K, Lis T, Bogucka M, Lutomska J, Kraszewski A. Different nucleobase orientations in two cyclic 2',3'-phosphates of purine ribonucleosides: Et(3)NH(2',3'-cAMP) and Et(3)NH(2',3'-cGMP)xH(2)O. Acta Crystallographica. Section C, Crystal Structure Communications. 62: o405-9. PMID 16823215 DOI: 10.1107/S0108270106017811 |
0.424 |
|
| 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 |
0.824 |
|
| 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 |
0.653 |
|
| 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 |
0.858 |
|
| 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 |
0.8 |
|
| 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 |
0.833 |
|
| 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 |
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 |
0.844 |
|
| 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 |
0.741 |
|
| 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 |
0.774 |
|
| 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 |
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 |
0.758 |
|
| 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 |
0.743 |
|
| 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 |
0.827 |
|
| 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 |
0.867 |
|
| 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 |
0.732 |
|
| 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 |
0.704 |
|
| 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 |
0.777 |
|
| 2002 |
Stawinski J, Kraszewski A. H-Phosphonates – chemistry and applications Collection of Czechoslovak Chemical Communications. 5: 272-282. DOI: 10.1135/Css200205272 |
0.736 |
|
| 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 |
0.761 |
|
| 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 |
0.86 |
|
| 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 |
0.859 |
|
| 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 |
0.669 |
|
| 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 |
0.786 |
|
| 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 |
0.836 |
|
| 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 |
0.779 |
|
| 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 |
0.697 |
|
| 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 |
0.641 |
|
| 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 |
0.747 |
|
| 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 |
0.775 |
|
| 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 |
0.717 |
|
| 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 |
0.761 |
|
| 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 |
0.687 |
|
| 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 |
0.786 |
|
| 1999 |
Kers I, Kers A, Stawiński J, Kraszewski A. Aryl Hphosphonates. 8. Simple and efficient method forv the preparation of nucleoside Hphosphonothioate monoesters Tetrahedron Letters. 40: 3945-3948. DOI: 10.1016/S0040-4039(99)00617-6 |
0.755 |
|
| 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 |
0.792 |
|
| 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 |
0.763 |
|
| 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 |
0.812 |
|
| 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 |
0.762 |
|
| 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 |
0.777 |
|
| 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 |
0.78 |
|
| 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 |
0.653 |
|
| 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 |
0.866 |
|
| 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 |
0.78 |
|
| 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 |
0.762 |
|
| 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 |
0.737 |
|
| 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 |
0.851 |
|
| 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 |
0.852 |
|
| 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 |
0.836 |
|
| 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 |
0.786 |
|
| 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 |
0.863 |
|
| 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 |
0.865 |
|
| 1995 |
Sobkowski M, Stawinki J, Sobkowska A, Kraszewski A. Studies on Reactions of Nucleoside H-Phosphonates with Bifunctional Reagents. Part III. Further Studies on Transesterification of Nucleoside H-Phosphonate Diesters with Amino Alcohols Nucleosides, Nucleotides and Nucleic Acids. 14: 839-842. DOI: 10.1080/15257779508012484 |
0.82 |
|
| 1995 |
Sobkowska A, Sobkowski M, Stawidski J, Kraszewski A. Studies on Aryl H-Phosphonates. Synthesis of Nucleoside N-Alkylphosphonamidates Nucleosides, Nucleotides and Nucleic Acids. 14: 703-706. DOI: 10.1080/15257779508012453 |
0.861 |
|
| 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 |
0.856 |
|
| 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 |
0.824 |
|
| 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 |
0.829 |
|
| 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 |
0.858 |
|
| 1993 |
Kraszewski A. The reactions of nucleoside H-phosphonates with amino alcohols Collection of Czechoslovak Chemical Communications. 58: 224. DOI: 10.1135/cccc1993s224 |
0.33 |
|
| 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 |
0.726 |
|
| 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 |
0.651 |
|
| 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 |
0.802 |
|
| 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 |
0.632 |
|
| 1980 |
KRASZEWSKI A, STAWINSKI J. ChemInform Abstract: PHOSPHORYL TRIS-THIAZOLE - A NEW PHOSPHORYLATING REAGENT Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198042278 |
0.571 |
|
| 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 |
0.794 |
|
| 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 |
0.64 |
|
| 1976 |
Adamiak RW, Barciszewska MZ, Biala E, Grzéskowiak K, Kierzek R, Kraszewski A, Markiewicz WT, Wiewiórowski M. Nucleoside-3'-phosphotriesters as key intermediates for the oligoribonucleotide synthesis. III. An improved preparation of nucleoside 3'-phosphotriesters, their 1H NMR characterization and new conditions for removal of 2-cyanoethyl group. Nucleic Acids Research. 3: 3397-408. PMID 1005124 DOI: 10.1093/Nar/3.12.3397 |
0.772 |
|
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