FACILE PRODUCTION AND CYCLIZATIONS OF AMIDYL RADICALS

DOI: 10.1016/S0040-4039(00)74480-7

Source and publish data:

Tetrahedron Letters p. 1035 - 1038 (1991)

Update date:2022-07-29

Topics:

Authors:

Newcomb, Martin

Esker, John L.

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Article abstract of DOI:10.1016/S0040-4039(00)74480-7

Amides were converted via imidoyl chlorides into N-hydroxypyridine-2-thione imidate esters that were precursors for amidyl radicals; amidyl radicals containing δ,ε-unsaturation cyclized in a 5-exo fashion.

Full text of DOI:10.1016/S0040-4039(00)74480-7

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