AMINOBOROHYDRIDES .8. A FACILE REDUCTION OF ALIPHATIC AND BENZYLIC AZIDES TO THE CORRESPONDING AMINES IN HIGH-YIELD AND PURITY USING LITHIUM N,N-DIMETHYLAMINOBOROHYDRIDE

Citation
Sg. Alvarez et al., AMINOBOROHYDRIDES .8. A FACILE REDUCTION OF ALIPHATIC AND BENZYLIC AZIDES TO THE CORRESPONDING AMINES IN HIGH-YIELD AND PURITY USING LITHIUM N,N-DIMETHYLAMINOBOROHYDRIDE, Tetrahedron letters, 36(15), 1995, pp. 2567-2570
Citations number
36
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
36
Issue
15
Year of publication
1995
Pages
2567 - 2570
Database
ISI
SICI code
0040-4039(1995)36:15<2567:A.AFRO>2.0.ZU;2-8
Abstract
Lithium N,N-dimethylaminoborohydride (LiMe(2)NBH(3)) reduced both 3 al pha-azidocholest-5-ene and 3 beta-azidocholest-5-ene in air to give th e corresponding 3 alpha-aminocholest-5-ene and 3 beta-aminocholest-5-e ne in 98% isolated yields. Aliphatic and benzylic azides were also red uced with LiMe(2)NBH(3) to give the corresponding amines in isolated y ields ranging from 85 to 98%. The reductions were complete in 1-3 hour s and required only a simple acid-base extraction to isolate the desir ed amines.