TANDEM ZINC MEDIATED REDUCTIVE CLEAVAGE REDUCTIVE AMINATION AS A NEW APPROACH TO SUBSTITUTED PYRROLIDINES FROM HOMOALLYLIC AMINES

Citation
C. Vanucci et al., TANDEM ZINC MEDIATED REDUCTIVE CLEAVAGE REDUCTIVE AMINATION AS A NEW APPROACH TO SUBSTITUTED PYRROLIDINES FROM HOMOALLYLIC AMINES, Tetrahedron letters, 36(17), 1995, pp. 2971-2974
Citations number
7
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
36
Issue
17
Year of publication
1995
Pages
2971 - 2974
Database
ISI
SICI code
0040-4039(1995)36:17<2971:TZMRCR>2.0.ZU;2-H
Abstract
N-Boc or N-Cbz homoallylic amines are converted in four steps into pyr rolidines through a sequence involving as a key-step a tandem zinc med iated reductive cleavage-reductive amination from an intermediate 1,3- oxazin-2-one