95482-67-0

Upstream product

• 102254-73-9 Dimethylamino-[(E)-thiobenzoylimino]-acetic acid ethyl ester 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 87108-97-2 4-dimethylamino-4-ethoxycarbonyl-1-thia-3-aza-2-C₆H₅-butadiene 

Downstream Products

• 134857-33-3 2-ethyl 3,4-dimethyl 5-phenyl-1H-pyrrole-2,3,4-tricarboxylate 
• 142178-48-1 5-aza-4-ethoxycarbonyl-3-methoxycarbonyl-6-phenyl-6-thioxo-hexanoate de methyle 
• 142178-46-9 4-ethoxycarbonyl-5-methoxycarbonyl-5-methoxycarbonylmethyl-2-phenyl-2-thiazoline 

Relevant academic research and scientific papers

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

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

Reduction electrochimique de 4H-1,3-thiazines : obtention de 6H-1,3-thiazines et (ou) de pyrroles substitues

Controlled potential electroreduction (protic medium, mercury cathode) of substituted 2-ethoxy and 2-phenyl-4H-1,3-thiazines leads to 6H-1,3-thiazines and (or) pyrroles.The nature of the isolated products appears strongly dependent on pH of the medium and