CHIRAL SYNTHONS FROM CARVONE .26. SYNTHESIS OF CHIRAL BICYCLO[3.3.1]NONANES VIA A TANDEM INTERMOLECULAR ALKYLATION-INTRAMOLECULAR MICHAEL REACTION SEQUENCE

Authors
SRIKRISHNA A REDDY TJ KUMAR PP
Citation
A. Srikrishna et al., CHIRAL SYNTHONS FROM CARVONE .26. SYNTHESIS OF CHIRAL BICYCLO[3.3.1]NONANES VIA A TANDEM INTERMOLECULAR ALKYLATION-INTRAMOLECULAR MICHAEL REACTION SEQUENCE, Synlett, (6), 1997, pp. 663-664
Citations number
10
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
6
Year of publication
1997
Pages
663 - 664
Database
ISI
SICI code
0936-5214(1997):6<663:CSFC.S>2.0.ZU;2-5
Abstract
Stereo- and regioselective synthesis of chiral bicyclo-[3.3.1]nonanes employing a tandem intermolecular alkylation and intramolecular Michae l reaction sequence, starting from 10-bromocarvone derivatives and Mic hael donors is described.