Highly stereoselective intramolecular α-arylation of self-stabilized non-racemic enolates: synthesis of α-quaternary α-amino acid derivatives?

Chemical Communications Pub Date: 2009-07-13 DOI: 10.1039/B910326K

Abstract

The ‘one-pot’ stereoselective conversion of N-(4-nitrobenzene)sulfonyl-α-amino acid tert-butyl esters into the corresponding N-alkyl-α-(4-nitrophenyl)-α-amino esters has been realized through N-alkylation of the starting amido esters, followed by N–Cα migration of the p-nitrophenyl group and the loss of sulfur dioxide; the asymmetric induction is determined by an intermediate non-racemic enolate, without the need of an external source of chirality.

Graphical abstract: Highly stereoselective intramolecular α-arylation of self-stabilized non-racemic enolates: synthesis of α-quaternary α-amino acid derivatives
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