Desymmetrization of myo-inositol

TitleDesymmetrization of myo-inositol
Publication TypeJournal Article
Year of Publication2025
AuthorsPatil, NT, Patil, MT, Gonnade, RG, Shashidhar, MS
JournalCarbohydrate Research
Volume553
Pagination109505
Date PublishedJUL
Type of ArticleArticle
ISSN0008-6215
KeywordsConglomerate, Crystallization, Cyclitol, Enantiomers, Inositol, Lipid
Abstract

Chemistry and biology of phosphoinositols have been intensely investigated areas of research over the last 4-5 decades due to their involvement in cellular signal transduction pathways. Efficient laboratory synthesis of enantiomeric derivatives of inositols was a central issue since they were required for the delineation of the myo-inositol cycle as well as for the total synthesis of polyol based natural products and their derivatives. This essentially meant the development of competent methods for the desymmetrization of myo-inositol leading to the preparation of enantiomeric O-substituted derivatives of myo-inositol. This was approached by: the classical resolution methods involving separable diastereomers, the chiral pool synthesis, enzyme catalysis, asymmetric catalysis and preferential crystallization of enantiomers in a racemic conglomerate. This review summarizes results obtained in author's laboratory, as well as those reported in the literature on attempts at desymmetrization of myo-inositol.

DOI10.1016/j.carres.2025.109505
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

2.5

Divison category: 
Organic Chemistry
Physical and Materials Chemistry
Database: 
Web of Science (WoS)

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