INTRAMOLECULAR CYCLOADDITIONS USING VINYL SULFIDE DIENOPHILES

DOI: 10.1016/S0040-4039(00)84291-4

Source and publish data:

Tetrahedron Letters p. 1485 - 1488 (1986)

Update date:2022-08-03

Topics:

Authors:

Williams, D.R.

Gaston, R.D.

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Article abstract of DOI:10.1016/S0040-4039(00)84291-4

The formation of hexahydrobenzo(b)thiophenes have been examined by a Diels-Alder route featuring a vinylic sulfide as the dienophilic component.Unique aspects of the observed stereoselectivity and further stereochemical transformations are presented.

Full text of DOI:10.1016/S0040-4039(00)84291-4

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