☆ 4.7 Article

Asymmetric deprotonation and dearomatising cyclisation of N-benzyl benzamides using chiral lithium amides: formal synthesis of (-)-kainic acid

CHEMICAL COMMUNICATIONS (2002)

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CHEMICAL COMMUNICATIONS

Volume -, Issue 1, Pages 38-39

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ROYAL SOC CHEMISTRY

DOI: 10.1039/b109188c

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Abstract

Chiral lithium amides deprotonate N-benzyl benzamides enantioselectively, initiating an asymmetric dearomatising cyclisation to enantiomerically enriched isoindolinones.

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Asymmetric deprotonation and dearomatising cyclisation of N-benzyl benzamides using chiral lithium amides: formal synthesis of (-)-kainic acid

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CHEMICAL COMMUNICATIONS

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ROYAL SOC CHEMISTRY

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Asymmetric deprotonation and dearomatising cyclisation of N-benzyl benzamides using chiral lithium amides: formal synthesis of (-)-kainic acid

Journal

CHEMICAL COMMUNICATIONS

Publisher

ROYAL SOC CHEMISTRY

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