Enantioselective synthesis of alpha-methyl-beta-aminoacid derivatives via aza-aldol reaction of acylcamphorsultam enolates

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McLaren, Andrew and Sweeney, Joseph B. (2000) Enantioselective synthesis of alpha-methyl-beta-aminoacid derivatives via aza-aldol reaction of acylcamphorsultam enolates. Synlett, 11. pp. 1625-1627. ISSN 0936-5214

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Official URL: http://dx.doi.org/10.1055/s-2000-7926

DOI: 10.1055/s-2000-7926

Abstract

The aza-aldol reaction of the chiral enolate derived from (2S)-N-propionoyl camphor sultam 1 with certain N-diphenylphosphinyl imines furnishes N-(2R, 3R-α-methyl-β-diphosphinylamido)acylsultams, in acceptable to good yields and with virtually complete diastereo- and enantiocontrol. The method represents an operationally-simple route for preparation of α-methyl-β-aminoacids from readily-available starting materials.

Item Type:	Article
Subjects:	Q Science > QD Chemistry
Schools:	School of Applied Sciences
Related URLs:	Author
Depositing User:	Joseph Sweeney
Date Deposited:	18 Oct 2012 11:30
Last Modified:	18 Oct 2012 11:30
URI:	http://eprints.hud.ac.uk/id/eprint/15290

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