Determination of the absolute configuration of gliomasolide D through total syntheses of the C-17 epimers
Title | Determination of the absolute configuration of gliomasolide D through total syntheses of the C-17 epimers |
Publication Type | Journal Article |
Year of Publication | 2017 |
Authors | Seetharamsingh, B, Ganesh, R, D. Reddy, S |
Journal | Journal of Natural Products |
Volume | 80 |
Issue | 2 |
Pagination | 560-564 |
Date Published | FEB |
Abstract | The 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. |
DOI | 10.1021/acs.jnatprod.6b00926 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 3.662 |
Divison category:
Organic Chemistry
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