A SYNTHETIC ROUTE TO ANTI-AMINOALKYL EPOXIDES BY STEREOCONTROLLED REDUCTIVE AMINATION OF KETOEPOXIDES

Authors
PEGORIER L PETIT Y LARCHEVEQUE M
Citation
L. Pegorier et al., A SYNTHETIC ROUTE TO ANTI-AMINOALKYL EPOXIDES BY STEREOCONTROLLED REDUCTIVE AMINATION OF KETOEPOXIDES, Journal of the Chemical Society, Chemical Communications, (5), 1994, pp. 633-634
Citations number
33
Categorie Soggetti
Chemistry
Journal title
Journal of the Chemical Society, Chemical Communications → ACNP
ISSN journal
00224936
Issue
5
Year of publication
1994
Pages
633 - 634
Database
ISI
SICI code
0022-4936(1994):5<633:ASRTAE>2.0.ZU;2-M
Abstract
anti-Aminoalkyl epoxides are synthesized in an enantiomerically pure f orm by stereoselective reductive amination of ketoepoxides derived fro m methyl glycidate with tetramethylammonium triacetoxyborohydride.