Diastereoselective pentadienylation reaction of protected chiral alpha-amino aldehydes

Citation
F. Minassian et al., Diastereoselective pentadienylation reaction of protected chiral alpha-amino aldehydes, SYNLETT, (2), 2000, pp. 242-244
Citations number
25
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
2
Year of publication
2000
Pages
242 - 244
Database
ISI
SICI code
0936-5214(200002):2<242:DPROPC>2.0.ZU;2-F
Abstract
Diastereoselective pentadienylation of chiral a-amino aldehydes was achieve d. The obtained anti amino alcohols can be transformed into dienic imines w hich undergo Diels-Alder cyclisation to give stereoselectively indolizidine s.