RESERPINE SYNTHESIS - A PROTOCOL FOR THE STEREOSELECTIVE CONSTRUCTIONOF THE DENSELY FUNCTIONALIZED RING-E

Authors
MEHTA G REDDY DS
Citation
G. Mehta et Ds. Reddy, RESERPINE SYNTHESIS - A PROTOCOL FOR THE STEREOSELECTIVE CONSTRUCTIONOF THE DENSELY FUNCTIONALIZED RING-E, Journal of the Chemical Society. Perkin transactions. I (Print), (14), 1998, pp. 2125-2126
Citations number
19
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I (Print) → ACNP
ISSN journal
0300922X
Issue
14
Year of publication
1998
Pages
2125 - 2126
Database
ISI
SICI code
0300-922X(1998):14<2125:RS-APF>2.0.ZU;2-H
Abstract
A new approach to densely functionalized cyclohexanoid derivative 12, embodying the complete stereochemical pattern of ring-E of the complex indole alkaloid reserpine 1, from a readily available tricycle [5.2.1 .0(2,6)] decane precursor 5 is described.