Issue 12, 1996

An expedient preparation of chiral building blocks having levoglucosenone chromophore: a new enanticontrolled route to (–)-β-multistriatin and (+)-exo-brevicomin

Abstract

2-Alkenylfurans are transformed enantioselectively into the bicyclic enones having the levoglucosenone chromophore, whose synthetic utility is demonstrated by a stereocontrolled synthesis of two insect pheromones (–)-β-multistriatin and (+)-exo-brevicomin.

Article information

Article type
Paper

Chem. Commun., 1996, 1477-1478

An expedient preparation of chiral building blocks having levoglucosenone chromophore: a new enanticontrolled route to (–)-β-multistriatin and (+)-exo-brevicomin

T. Taniguchi, H. Ohnishi and K. Ogasawara, Chem. Commun., 1996, 1477 DOI: 10.1039/CC9960001477

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