A selective electrochemical way to functionalized 6H-1,3-thiazines and/or pyrroles

DOI: 10.1016/S0040-4039(00)79687-0

Source and publish data:

Tetrahedron Letters p. 2225 - 2228 (1991)

Update date:2022-08-05

Topics:

Authors:

Abouelfida

Jubault Jubault

Pradere Pradere

Roze Roze

Tallec Tallec

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Article abstract of DOI:10.1016/S0040-4039(00)79687-0

4H-1,3-thiazines, easily prepared from 1-thia-3-azabutadienes, appear electroactive in protic medium. Controlled potential electroreductions of 4H-1,3-thiazines lead either to substituted 6H-1,3-thiazines or to pyrroles according to the nature of the C-4

Full text of DOI:10.1016/S0040-4039(00)79687-0

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Product name:4H-1,3-Thiazine-4,5,6-tricarboxylic acid, 4-(dimethylamino)-2-phenyl-, 4-ethyl 5,6-dimethyl ester

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