Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5272939 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
The total synthesis of (+)-(6R,2â²S)-cryptocaryalactone and (â)-(6S,2â²S)-epi cryptocaryalactone is reported based on asymmetric acetate aldol reaction. Still-Gennari reaction, Evans acetal intramolecular oxa-Michael reaction and lactonisation are the key steps in the target synthesis.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
J.S. Yadav, Dinesh C. Bhunia, B. Ganganna,