Substrate dependent intramolecular Pauson-Khand reaction of carbohydrate exo-methylene derivatives. Unexpected formation of fused '[4.1.0] bicycloheptene - pyranose' tricyclic product

DOI: 10.1016/0040-4039(96)00046-9

Source and publish data:

Tetrahedron Letters p. 1489 - 1492 (1996)

Update date:2022-07-31

Topics:

Authors:

Borodkin

Shpiro Shpiro

Azov Azov

Kochetkov

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Article abstract of DOI:10.1016/0040-4039(96)00046-9

Attempted Pauson-Khand cyclisation of exo- methylene carbohydrate enynic substrates is described. 3-Exo methylene derivative cyclises to give a normal Pauson-Khand product while cyclisation of a 4-exo methylene analog follows a previously unreported pathway to give fused '[4.1.0] bicycloheptene - pyranose' tricyclic product.

Full text of DOI:10.1016/0040-4039(96)00046-9

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