| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5220113 | Tetrahedron | 2011 | 5 Pages |
Abstract
A stereoselective total synthesis of (â)-cleistenolide (1) derived from d-(â)-isoascorbic acid has been described. The new synthetic strategy involves highly diastereoselective reduction, one-pot protection of required benzoyl, acetyl groups, and the RCM reaction by using Grubbs catalyst are the key steps with considerable yields.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Dokuburra Chanti Babu, Jondoss Jon Paul Selavam, Dorigondla Kumar Reddy, Vanam Shekhar, Yenamandra Venkateswarlu,