Issue 2, 1998

Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives

Abstract

Regioselective Dieckmann cyclisations using an N-acyloxazolidine derived from L-serine give substituted tetramic acids in high yield and enantioselectivity. The products are easily deprotected under mild conditions to give hydroxymethyltetramic acids.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 223-236

Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives

M. D. Andrews, A. G. Brewster, K. M. Crapnell, A. J. Ibbett, T. Jones, M. G. Moloney, K. Prout and D. Watkin, J. Chem. Soc., Perkin Trans. 1, 1998, 223 DOI: 10.1039/A706014I

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