Issue 8, 1998

Diastereoselective intramolecular nitroaldol entry to lycoricidine alkaloids

Abstract

The alumina promoted 6-exo-trig intramolecular nitroaldol cyclization described proceeds in a highly diastereoselective manner via a proposed chelation controlled chair-like transition state, the major diastereomer having the correct relative configuration at three stereocentres as observed in the pancratistatin series of antitumor agents, in contrast to prior literature cyclization methods.

Article information

Article type
Paper

Chem. Commun., 1998, 933-934

Diastereoselective intramolecular nitroaldol entry to lycoricidine alkaloids

J. McNulty and R. Mo, Chem. Commun., 1998, 933 DOI: 10.1039/A800097B

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