Synthesis of D-myo-inositol 3,4,5,6- and 1,4,5,6-tetrakisphosphate analogues and their membrane-permeant derivatives

Stefan Roemer, Marco T. Rudolf, Christoph Stadler, Carsten Schultz

Research output: Contribution to journalArticle

12 Scopus citations

Abstract

A set of D-myo-inositol 3,4,5,6- and 1,4,5,6-tetrakisphosphates [D-Ins(3,4,5,6)P4 and D-Ins(1,4,5,6)P4, respectively] analogues with modifications of the hydroxy groups is synthesized and subsequently converted to the corresponding uncharged, bioactivatable acetoxymethyl esters.

Original languageEnglish (US)
Pages (from-to)411-412
Number of pages2
JournalJournal of the Chemical Society, Chemical Communications
Issue number4
DOIs
StatePublished - Dec 1 1995

ASJC Scopus subject areas

  • Molecular Medicine

Fingerprint Dive into the research topics of 'Synthesis of D-myo-inositol 3,4,5,6- and 1,4,5,6-tetrakisphosphate analogues and their membrane-permeant derivatives'. Together they form a unique fingerprint.

  • Cite this