Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives

MD Andrews, AG Brewster, KM Crapnell…

Index: Andrews, Mark D.; Brewster, Andrew G.; Crapnell, Katherine M.; Ibbett, Ashley J.; Jones, Tim; Moloney, Mark G.; Prout, Keith; Watkin, David Journal of the Chemical Society - Perkin Transactions 1, 1998 , # 2 p. 223 - 235

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Citation Number: 52

Abstract

J. Chem. Soc., Perkin Trans. 1, 1998 223 ... Regioselective Dieckmann cyclisations leading to enantiopure highly ... Mark D. Andrews,a Andrew G. Brewster,c Katherine M. Crapnell,a Ashley J. Ibbett,b Tim Jones,b Mark G. Moloney,*,†,a Keith Proutb and David Watkinb ... 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 ...