Issue 13, 1986

Stereoselective synthesis of pyrrolizidine alkaloids via substituted nitrones

Abstract

The 3,5-disubstituted pyrrolizidine alkaloid (8) has been synthesised using, as a key step, the cyclisation of the allenic oxime E-(3) to generate a 5-substituted nitrone (4); under the same cyclisation conditions Z-(3) reacts via oxygen to give (9).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 1017-1018

Stereoselective synthesis of pyrrolizidine alkaloids via substituted nitrones

D. Lathbury and T. Gallagher, J. Chem. Soc., Chem. Commun., 1986, 1017 DOI: 10.1039/C39860001017

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