Literature DB >> 3697124

Evaluation of some new condensing reagents for hydrogenphosphonate diester formation.

R Strömberg1, J Stawinski.   

Abstract

Various pivaloyltetrazoles and chlorophosphates have been investigated as potential condensing reagents for H-phosphonate diester formation. Acylating or phosphorylating properties as well as possible side-reactions triggered by these reagents were checked using TLC and 31P NMR analysis.

Entities:  

Mesh：

Substances：

Year:  1987        PMID： 3697124

Source DB:  PubMed          Journal:  Nucleic Acids Symp Ser        ISSN： 0261-3166


  2 in total

1.  One-flask syntheses of c-di-GMP and the [Rp,Rp] and [Rp,Sp] thiophosphate analogues.

Authors:  Barbara L Gaffney; Elizabeth Veliath; Jianwei Zhao; Roger A Jones
Journal:  Org Lett       Date:  2010-07-16       Impact factor: 6.005

2.  Studies on the t-butyldimethylsilyl group as 2'-O-protection in oligoribonucleotide synthesis via the H-phosphonate approach.

Authors:  J Stawinski; R Strömberg; M Thelin; E Westman
Journal:  Nucleic Acids Res       Date:  1988-10-11       Impact factor: 16.971
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.