Determination of the absolute configuration of gliomasolide D through total syntheses of the C-17 epimers

TitleDetermination of the absolute configuration of gliomasolide D through total syntheses of the C-17 epimers
Publication TypeJournal Article
Year of Publication2017
AuthorsSeetharamsingh, B, Ganesh, R, D. Reddy, S
JournalJournal of Natural Products
Volume80
Issue2
Pagination560-564
Date PublishedFEB
AbstractThe absolute configuration at C-17, the carbon bearing the distal hydroxy group of the 14-membered natural product gliomasolide D, was assigned as R by comparison of C-13 NMR shifts and specific rotation values of the epimers at C-17. The first total synthesis of gliomasolide D along with its C-17 epimer, regioselective macrocyclization (18 membered vs 14 membered), and regioselective Wacker oxidation are highlights of the present work.
DOI10.1021/acs.jnatprod.6b00926
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

3.662

Divison category: 
Organic Chemistry

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