User profiles for "author:Stawinski author:J."
 | Jacek StawinskiStockholm University Verified email at organ.su.se Cited by 6052 |
Arylsulfonyltetrazoles, new coupling reagents and further improvements in the triester method for the synthesis of deoxyribooligonucleotides1
J Stawinski, T Hozumi, SA Narang… - Nucleic acids …, 1977 - academic.oup.com
The modified triester approach has been further improved and refined to the synthesis of
defined sequences of deoxyribooligonucleotides. Improvements include
arylsulfonyltetrazoles as faster and milder condensing agents, benzenesulfonic acid to avoid …
defined sequences of deoxyribooligonucleotides. Improvements include
arylsulfonyltetrazoles as faster and milder condensing agents, benzenesulfonic acid to avoid …
[CITATION][C] Nucleoside H-phosphonates. III. Chemical synthesis of oligodeoxyribonucleotides by the hydrogenphosphonate approach
PJ Garegg, I Lindh, T Regberg, J Stawinski… - Tetrahedron letters, 1986 - Elsevier
Page 1. Tetrahedron Letters,Vo1.27,No.34,pp 4051-4054,1986 0040-4039/86 $3.00 +
.oo Printed in Great Britain Pergamon Journals Ltd. NUCLEOSIDE H-PHOSPHONATES.
III. CHEMICAL SYNTHESIS OF OLIGODEOXYRIBONUCLEOTIDES BY THE …
.oo Printed in Great Britain Pergamon Journals Ltd. NUCLEOSIDE H-PHOSPHONATES.
III. CHEMICAL SYNTHESIS OF OLIGODEOXYRIBONUCLEOTIDES BY THE …
[CITATION][C] Formation of Internucleotidic Bonds via Phosphonate Intermediates.
PJ Garegg, T Regberg, J Stawinski… - Chemischer …, 1986 - Wiley Online Library
Nucleoside H-phosphonates. IV. Automated solid phase synthesis of oligoribonucleotides by the hydrogenphosphonate approach
PJ Garegg, I Lindh, T Regberg, J Stawinski… - Tetrahedron letters, 1986 - Elsevier
A rapid and efficient synthesis of oligoribonucleotides on solid support is described via
coupling of 5′-O-dimethoxytrityl-2′-Ot-butyldimethylsilyl ribonucleoside 3′-H-
phosphonates II to the polymer bound nucleoside in the presence of pivaloyl chloride as …
coupling of 5′-O-dimethoxytrityl-2′-Ot-butyldimethylsilyl ribonucleoside 3′-H-
phosphonates II to the polymer bound nucleoside in the presence of pivaloyl chloride as …
[CITATION][C] Nucleoside Hydrogenphosphonates in Oligonucleotide Synthesis.
PJ Garegg, T Regberg, J Stawinski… - Chemischer …, 1986 - Wiley Online Library
How to get the most out of two phosphorus chemistries. Studies on H-phosphonates
J Stawinski, A Kraszewski - Accounts of chemical research, 2002 - ACS Publications
The biological importance and practical significance of phosphate esters and their
analogues have been the major driving forces for research in various areas of synthetic
organic phosphorus chemistry. In this Account, the authors' studies on the development of a …
analogues have been the major driving forces for research in various areas of synthetic
organic phosphorus chemistry. In this Account, the authors' studies on the development of a …
Microwave-assisted palladium-catalyzed cross-coupling of aryl and vinyl halides with H-phosphonate diesters
M Kalek, A Ziadi, J Stawinski - Organic letters, 2008 - ACS Publications
A general and efficient method for the microwave-assisted formation of the C− P bond was
developed. Using a prevalent palladium catalyst, Pd (PPh3) 4, a quantitative cross-coupling
of various H-phosphonate diesters with aryl and vinyl halides was achieved in less than 10 …
developed. Using a prevalent palladium catalyst, Pd (PPh3) 4, a quantitative cross-coupling
of various H-phosphonate diesters with aryl and vinyl halides was achieved in less than 10 …
A general method for the synthesis of glycerophospholipids and their analogs via H-phosphonate intermediates
I Lindh, J Stawinski - The Journal of Organic Chemistry, 1989 - ACS Publications
A general chemical method for the synthesis of glycerophospholipids and their analogues
via H-phosphonate intermediates has been developed. It was found that l, 2-
dipalmitoylglycero-3-H-phosphonate, prepared by the reaction of 1, 2-dipalmitoylglycerol …
via H-phosphonate intermediates has been developed. It was found that l, 2-
dipalmitoylglycero-3-H-phosphonate, prepared by the reaction of 1, 2-dipalmitoylglycerol …
Studies on aryl H-phosphonates. I. An efficient method for the preparation of deoxyribo-and ribonucleoside 3′-H-phosphonate monoesters by transesterification of …
J Jankowska, M Sobkowski, J Stawiński, A Kraszewski - Tetrahedron letters, 1994 - Elsevier
InstiMe of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12/14,6 I-704
Pomti, Poland … Abstract: A convenient method for the preparation of deoxyribonucleoside
and ribonucleoside 3'-H-phosphonate monoesters via transesterification of diphenyl H-phosphonate …
Pomti, Poland … Abstract: A convenient method for the preparation of deoxyribonucleoside
and ribonucleoside 3'-H-phosphonate monoesters via transesterification of diphenyl H-phosphonate …
Arylsulfonyltetrazoles as highly efficient condensing reagents for polynucleotide synthesis
J Stawinski, T Hozumi… - Canadian Journal of …, 1976 - NRC Research Press
J. STAWINSKI, T. HOZUMI, and S. A. NARANG. Can. J. Chem. 54,670 (1976). Various arylsulfonyltetrazoles
have been investigated to build the phosphotriester bond between appropriately protected
oligonucleotides. These reagents have been found to be highly effective with respect to the time …
have been investigated to build the phosphotriester bond between appropriately protected
oligonucleotides. These reagents have been found to be highly effective with respect to the time …
