The asymmetric synthesis of beta-haloaryl-beta-amino acid derivatives

Lithium N-benzyl-N-α-methyl-4-methoxybenzylamide is employed as a homochiral ammonia equivalent for the asymmetric synthesis of β-haloaryl-β-amino acid derivatives using a conjugate addition/oxidative deprotection strategy.

Bibliographic Details
Main Authors:	Bull, S, Davies, S, Delgado-Ballester, S, Fenton, G, Kelly, P, Smith, A
Format:	Journal article
Language:	English
Published:	2000

Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives by Bull, S, Davies, S, Delgado-Ballester, S, Kelly, P, Kotchie, L, Gianotti, M, Laderas, M, Smith, A

Published 2001

Journal article

The asymmetric synthesis of beta-haloaryl-beta-amino acid derivatives

Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives by Bull, S, Davies, S, Delgado-Ballester, S, Kelly, P, Kotchie, L, Gianotti, M, Laderas, M, Smith, A

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