Alkylthionitroso and arylthionitroso compounds generated from N- trimethylsilyl-N-chlorothioalkylamine precursors

DOI: 10.1016/S0040-4039(00)77083-3

Source and publish data:

Tetrahedron Letters p. 5275 - 5278 (1994)

Update date:2022-07-31

Topics:

Authors:

Bryce Bryce

Chesney Chesney

Heaton Heaton

McKelvey

Anderson

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Article abstract of DOI:10.1016/S0040-4039(00)77083-3

A range of alkylthionitroso and arylthionitroso compounds have been generated by thermal fragmentation of N-trimethylsilyl-N- chlorothioalkyl(aryl)amine precursors, and intercepted by reaction with dimethylbutadiene to afford Diels-Alder and ene adducts.

Full text of DOI:10.1016/S0040-4039(00)77083-3

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