CHIRAL SYNTHONS FROM CARVONE .20. STEREOSPECIFIC AND ENANTIOSPECIFIC TOTAL SYNTHESIS OF (-)-VALERANONE

Authors
SRIKRISHNA A VISWAJANANI R
Citation
A. Srikrishna et R. Viswajanani, CHIRAL SYNTHONS FROM CARVONE .20. STEREOSPECIFIC AND ENANTIOSPECIFIC TOTAL SYNTHESIS OF (-)-VALERANONE, Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry, 35(6), 1996, pp. 521-523
Citations number
14
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry → ACNP
ISSN journal
03764699
Volume
35
Issue
6
Year of publication
1996
Pages
521 - 523
Database
ISI
SICI code
0376-4699(1996)35:6<521:CSFC.S>2.0.ZU;2-U
Abstract
Stereo- and enantiospecific total synthesis of the irregular sesquiter pene, valeranone, starting from S-6-methylcarvone employing a hydrinda none to decalone ring expansion methodology, is described.