Applications of homoallylic alcohols derived from (-)-sparteine-mediated asymmetric homoaldolization: Entry to 5-to 8-membered unsaturated oxacycles through metathesis reaction

Citation
Krk. Prasad et D. Hoppe, Applications of homoallylic alcohols derived from (-)-sparteine-mediated asymmetric homoaldolization: Entry to 5-to 8-membered unsaturated oxacycles through metathesis reaction, SYNLETT, (7), 2000, pp. 1067-1069
Citations number
36
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
7
Year of publication
2000
Pages
1067 - 1069
Database
ISI
SICI code
0936-5214(200007):7<1067:AOHADF>2.0.ZU;2-P
Abstract
A series of enantioenriched 4-hydroxy-1-alkenyl carbamates was prepared by (-)-sparteine-mediated homoaldolization. These were transformed into unsatu rated oxacycles, involving simple synthetic transformations, with ring-clos ing metathesis (RCM) as the key step.