Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. 5872-08-2, Name is (7,7-Dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonic acid, molecular formula is , belongs to thiazines compound. The appropriate choice of redox mediator can avoid electrode passivation and overpotential.In a document, author is Luo, Zhibin, Category: thiazines.
Trifluoroborane catalyzed chemoselective synthesis of highly functionalized 1,3-thiazin-2-ylidenes
An efficient chemoselective synthesis of 1,3-thiazine-2-ylidenes was achieved via annulations of beta-aroyl-thioacetamide with propargyl alcohols using BF(3)OEt(2)as Lewis acid catalyst. A broad spectrum of substrates was well tolerated under the mild reaction conditions producing desired thiazine heterocyclics in good yields.
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Reference:
Thiazine – an overview | ScienceDirect Topics,
,Thiazine | C4H5NS – PubChem