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Results: 1-25 | 26-28
Results: 1-25/28
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
Authors: Golos, B Dzik, JM Kazimierczuk, Z Ciesla, J Zielinski, Z Jankowska, J Kraszewski, A Stawinski, J Rode, W Shugar, D
Citation: B. Golos et al., Interaction of thymidylate synthase with the 5 '-thiophosphates, 5 '-dithiophosphates, 5 '-H-phosphonates and 5 '-S-thiosulfates of 2 '-deoxyuridine,thymidine and 5-fluoro-2 '-deoxyuridine, BIOL CHEM, 382(10), 2001, pp. 1439-1445
A new selenium-transferring reagent-triphenylphosphine selenide
Authors: Bollmark, M Stawinski, J
Citation: M. Bollmark et J. Stawinski, A new selenium-transferring reagent-triphenylphosphine selenide, CHEM COMMUN, (8), 2001, pp. 771-772
The case for configurational stability of H-phosphonate diesters in the presence of diazabicyclo[5.4.0]undec-7-ene (DBU)
Authors: Johansson, T Stawinski, J
Citation: T. Johansson et J. Stawinski, The case for configurational stability of H-phosphonate diesters in the presence of diazabicyclo[5.4.0]undec-7-ene (DBU), BIO MED CH, 9(9), 2001, pp. 2315-2322
A new method for the synthesis of nucleoside 2 ',3 '-O,O-cyclic phosphorodithioates via aryl cyclic phosphites as intermediates
Authors: Wenska, M Jankowska, J Sobkowski, M Stawinski, J Kraszewski, A
Citation: M. Wenska et al., A new method for the synthesis of nucleoside 2 ',3 '-O,O-cyclic phosphorodithioates via aryl cyclic phosphites as intermediates, TETRAHEDR L, 42(45), 2001, pp. 8055-8058
2-Pyridylphosphonates: a new type of modification for nucleotide analogues
Authors: Johansson, T Kers, A Stawinski, J
Citation: T. Johansson et al., 2-Pyridylphosphonates: a new type of modification for nucleotide analogues, TETRAHEDR L, 42(11), 2001, pp. 2217-2220
Nucleoside phosphate analogues of biological interest, and their synthesisvia aryl nucleoside H-phosphonates as intermediates
Authors: Cieslak, J Sobkowski, M Jankowska, J Wenska, M Szymczak, M Imiolczyk, B Zagorowska, I Shugar, D Stawinski, J Kraszewski, A
Citation: J. Cieslak et al., Nucleoside phosphate analogues of biological interest, and their synthesisvia aryl nucleoside H-phosphonates as intermediates, ACT BIOCH P, 48(2), 2001, pp. 429-442
Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part VI. Reaction with diols
Authors: Sobkowski, M Wenska, M Kraszewski, A Stawinski, J
Citation: M. Sobkowski et al., Studies on reactions of nucleoside H-phosphonates with bifunctional reagents. Part VI. Reaction with diols, NUCLEOS NUC, 19(10-12), 2000, pp. 1487-1503
A new, efficient entry to nucleoside 2 ',3 '-O,O-cyclophosphorothioates
Authors: Jankowska, J Wenska, M Popenda, M Stawinski, J Kraszewski, A
Citation: J. Jankowska et al., A new, efficient entry to nucleoside 2 ',3 '-O,O-cyclophosphorothioates, TETRAHEDR L, 41(13), 2000, pp. 2227-2229
A simple and efficient method for direct acylation of acetals with long alkyl-chain carboxylic acid anhydrides
Authors: Stamatov, SD Stawinski, J
Citation: Sd. Stamatov et J. Stawinski, A simple and efficient method for direct acylation of acetals with long alkyl-chain carboxylic acid anhydrides, TETRAHEDRON, 56(49), 2000, pp. 9697-9703
Aryl H-phosphonates. 12. Synthetic and P-31 NMR studies on the preparationof nucleoside H-phosphonothioate and nucleoside H-phosphonodithioate monoesters
Authors: Cieslak, J Jankowska, J Stawinski, J Kraszewski, A
Citation: J. Cieslak et al., Aryl H-phosphonates. 12. Synthetic and P-31 NMR studies on the preparationof nucleoside H-phosphonothioate and nucleoside H-phosphonodithioate monoesters, J ORG CHEM, 65(21), 2000, pp. 7049-7054
Studies on enzymatic hydrolysis of thymidin-3 '-yl thymidin-5 '-yl phosphorofluoridates and the corresponding phosphorothiofluoridates
Authors: Misiura, K Bollmark, M Stawinski, J Stec, WJ
Citation: K. Misiura et al., Studies on enzymatic hydrolysis of thymidin-3 '-yl thymidin-5 '-yl phosphorofluoridates and the corresponding phosphorothiofluoridates, CHEM COMMUN, (20), 1999, pp. 2115-2116
Studies on the reaction of trityl derivatives with H-phosphonate diesters:Their relevance to the synthesis of 4-pyridylphosphonates
Authors: Kers, A Dembkowski, L Kraszewski, A Stawinski, J
Citation: A. Kers et al., Studies on the reaction of trityl derivatives with H-phosphonate diesters:Their relevance to the synthesis of 4-pyridylphosphonates, HETEROAT CH, 10(6), 1999, pp. 492-499
New methods for the formation of the P-N and P-F bonds, their relevance tonucleotide and oligonucleotide analogues synthesis
Authors: Kers, I Bollmark, M Kraszewski, A Stawinski, J
Citation: I. Kers et al., New methods for the formation of the P-N and P-F bonds, their relevance tonucleotide and oligonucleotide analogues synthesis, PHOSPHOR SU, 146, 1999, pp. 637-640
A mild method for the preparation of nucleoside phosphorofluoridate and phosphorofluoridothioate diesters
Authors: Bollmark, M Stawinski, J
Citation: M. Bollmark et J. Stawinski, A mild method for the preparation of nucleoside phosphorofluoridate and phosphorofluoridothioate diesters, NUCLEOS NUC, 18(6-7), 1999, pp. 1243-1244
New methods for multiple modifications of a phosphorus centre. Their relevance to nucleotide and oligonucleotide analogues synthesis
Authors: Kers, I Cieslak, J Jankowska, J Kraszewski, A Stawinski, J
Citation: I. Kers et al., New methods for multiple modifications of a phosphorus centre. Their relevance to nucleotide and oligonucleotide analogues synthesis, NUCLEOS NUC, 18(6-7), 1999, pp. 1245-1246
Aryl nucleoside H-phosphonates - Novel derivatives of controlled reactivity
Authors: Cieslak, J Jankowska, J Szymczak, M Kers, A Kers, I Stawinski, J Kraszewski, A
Citation: J. Cieslak et al., Aryl nucleoside H-phosphonates - Novel derivatives of controlled reactivity, NUCLEOS NUC, 18(4-5), 1999, pp. 937-938
P-31 NMR studies on oxidative transformations of aryl nucleoside H-phosphonate diesters
Authors: Kers, A Kers, I Cieslak, J Kraszewski, A Stawinski, J
Citation: A. Kers et al., P-31 NMR studies on oxidative transformations of aryl nucleoside H-phosphonate diesters, NUCLEOS NUC, 18(4-5), 1999, pp. 991-992
Synthesis and in vitro antiviral activity of some symmetrical phosphoramidate dimers of AZT
Authors: Kers, I Girardet, JL Gosselin, G Perigaud, C Imbach, JL Stawinski, J
Citation: I. Kers et al., Synthesis and in vitro antiviral activity of some symmetrical phosphoramidate dimers of AZT, NUCLEOS NUC, 18(4-5), 1999, pp. 993-994
Synthesis and anti-retroviral activity of O,O '-bis(3 '-azido-2 ',3 '-dideoxythymidin-5 '-yl) phosphoramidate derivatives
Authors: Kers, I Stawinski, J Girardet, JL Imbach, JL Perigaud, C Gosselin, G Aubertin, AM
Citation: I. Kers et al., Synthesis and anti-retroviral activity of O,O '-bis(3 '-azido-2 ',3 '-dideoxythymidin-5 '-yl) phosphoramidate derivatives, NUCLEOS NUC, 18(10), 1999, pp. 2317-2325
The reaction of diphenyl and dialkyl phosphorochloridates with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Formation of phosphonate diesters via N -> Cphosphorus migration
Authors: Kers, A Kers, I Stawinski, J
Citation: A. Kers et al., The reaction of diphenyl and dialkyl phosphorochloridates with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Formation of phosphonate diesters via N -> Cphosphorus migration, J CHEM S P2, (10), 1999, pp. 2071-2075
Aryl H-phosphonates. Part 11. Synthetic and P-31 NMR studies on the formation of aryl nucleoside H-phosphonates
Authors: Cieslak, J Szymczak, M Wenska, M Stawinski, J Kraszewski, A
Citation: J. Cieslak et al., Aryl H-phosphonates. Part 11. Synthetic and P-31 NMR studies on the formation of aryl nucleoside H-phosphonates, J CHEM S P1, (22), 1999, pp. 3327-3331
Preparation of nucleoside 5 '-deoxy-5 '-methylenephosphonates as building blocks for the synthesis of methylenephosphonate analogues
Authors: Kers, A Szabo, T Stawinski, J
Citation: A. Kers et al., Preparation of nucleoside 5 '-deoxy-5 '-methylenephosphonates as building blocks for the synthesis of methylenephosphonate analogues, J CHEM S P1, (18), 1999, pp. 2585-2590
A new type of nucleotide analogue with 4-pyridylphosphonate internucleotide linkage
Authors: Kers, A Stawinski, J
Citation: A. Kers et J. Stawinski, A new type of nucleotide analogue with 4-pyridylphosphonate internucleotide linkage, TETRAHEDR L, 40(22), 1999, pp. 4263-4266
Aryl H-phosphonates. 8. Simple and efficient method for the preparation ofnucleoside H-phosphonothioate monoesters
Authors: Kers, I Kers, A Stawinski, J Kraszewski, A
Citation: I. Kers et al., Aryl H-phosphonates. 8. Simple and efficient method for the preparation ofnucleoside H-phosphonothioate monoesters, TETRAHEDR L, 40(20), 1999, pp. 3945-3948
Aryl H-phosphonates. 10. Synthesis of nucleoside phosphoramidate and nucleoside phosphoramidothioate analogues via H-phosphonamidate intermediates
Authors: Kers, I Stawinski, J Kraszewski, A
Citation: I. Kers et al., Aryl H-phosphonates. 10. Synthesis of nucleoside phosphoramidate and nucleoside phosphoramidothioate analogues via H-phosphonamidate intermediates, TETRAHEDRON, 55(38), 1999, pp. 11579-11588
Risultati: 1-25 | 26-28