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

DOI: 10.1039/CC9960001477

Source and publish data:

Chemical Communications p. 1477 - 1478 (1996)

Update date:2022-07-29

Topics:

Authors:

Taniguchi, Takahiko

Ohnishi, Hiroshi

Ogasawara, Kunio

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Article abstract of DOI:10.1039/CC9960001477

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

Full text of DOI:10.1039/CC9960001477

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