Literature DB >> 31765170

Selective Transesterification of 2,2,2-Trifluoroethyl Phosphates: Synthesis of Mixed Unsymmetrical Phosphates.

Kouta Tsubaki1, Hirokazu Shimooka1, Mitsuru Kitamura1, Tatsuo Okauchi1.   

Abstract

A selective transesterification starting with tris(2,2,2-trifluoroethyl) phosphate has been developed. This method involves a three-step substitution for 2,2,2-trifluoroethoxy groups and enables the facile synthesis of mixed unsymmetric phosphate triesters from three different alcohols. The substitution of the trifluoroethoxy group at the phosphorus proceeds selectively in the presence of DBU or lithium alkoxides. This method can be applied for the preparation of phospholipids.

Entities:  

Year:  2019        PMID: 31765170     DOI: 10.1021/acs.orglett.9b04003

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  SiRNAs with Neutral Phosphate Triester Hydrocarbon Tails Exhibit Carrier-Free Gene-Silencing Activity.

Authors:  Matthew L Hammill; Kouta Tsubaki; Lidya Salim; Andrew J Varley; Ifrodet Giorgees; Mitsuru Kitamura; Tatsuo Okauchi; Jean-Paul Desaulniers
Journal:  ACS Med Chem Lett       Date:  2022-03-14       Impact factor: 4.632

2.  Synthesis and Evaluation of Neutral Phosphate Triester Backbone-Modified siRNAs.

Authors:  Kouta Tsubaki; Matthew L Hammill; Andrew J Varley; Mitsuru Kitamura; Tatsuo Okauchi; Jean-Paul Desaulniers
Journal:  ACS Med Chem Lett       Date:  2020-06-09       Impact factor: 4.345

  2 in total

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