Issue 12, 1991

Interception of an iminium ion equivalent by intramolecular nucleophilic attack by a silyl ether during lithium aluminium hydride reduction of a tertiary lactam

Abstract

The efficient formation of a bicyclic oxazolidine by lithium aluminium hydride reduction of a tertiary amide provides an example of intramolecular nucleophilic capture of an iminium ion equivalent by the oxygen of a silyl ether.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1991, 1991-1993

Interception of an iminium ion equivalent by intramolecular nucleophilic attack by a silyl ether during lithium aluminium hydride reduction of a tertiary lactam

N. G. Ramsden, G. W. J. Fleet and S. K. Namgoong, J. Chem. Soc., Perkin Trans. 2, 1991, 1991 DOI: 10.1039/P29910001991

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