REDUCTIVE DIALLYLATION OF NATURAL AMINO-ACIDS WITH TRIALLYLBORANE - THE FIRST SYNTHESIS OF CHIRAL 1,1-DIALLYL-2-AMINO ALCOHOLS AND THEIR CYCLIZATION INTO OPTICALLY-ACTIVE PYRROLIDINES

Authors
BUBNOV YN MISHARIN MA IGNATENKO AV
Citation
Yn. Bubnov et al., REDUCTIVE DIALLYLATION OF NATURAL AMINO-ACIDS WITH TRIALLYLBORANE - THE FIRST SYNTHESIS OF CHIRAL 1,1-DIALLYL-2-AMINO ALCOHOLS AND THEIR CYCLIZATION INTO OPTICALLY-ACTIVE PYRROLIDINES, Tetrahedron letters, 38(35), 1997, pp. 6259-6262
Citations number
22
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
38
Issue
35
Year of publication
1997
Pages
6259 - 6262
Database
ISI
SICI code
0040-4039(1997)38:35<6259:RDONAW>2.0.ZU;2-Y
Abstract
The titled amino alcohols are obtained by treatment of chiral amino ac ids with triallylborane. Electrophylic iodocyclization of the alcohols leads to pyrrolidine derivatives. (C) 1997 Elsevier Science Ltd.