Chemical Research Letters, May 2021. Redox catalysis has been broadly utilized in electrochemical synthesis. The appropriate choice of redox mediator can avoid electrode passivation, which strongly inhibit the efficient activation of substrates. 110553-27-0, Name is 2-Methyl-4,6-bis((octylthio)methyl)phenol, molecular formula is C25H44OS2. In an article, author is Cui, Jichun,once mentioned of 110553-27-0, Computed Properties of https://www.ambeed.com/products/110553-27-0.html.
Synthesis of imidazobenzothiazine and primidobenazothiazine derivatives via the classic Ullmann cross-coupling reaction of 1,8-diiodonaphthalene with 1H-benzo[d]imidazole-2-thiols or 2-thiouracils
A feasible protocol for the synthesis of imidazobenzothiazine and primidobenazothiazine derivatives via the classic copper(I)-catalyzed Ullmann cross-coupling process has been developed. 1,8-Diiodonaphthalene could couple with 2-mercaptobenzimidazoles or 2-thiouracils to give the corresponding benzo[4,5]imidazo[2,1-b]naphtho[1,8-de][1,3]thiazines and 11H-naphtho[1,8-de]pyrimido[2,1-b][1,3]thiazin-11-ones in moderate yields. [GRAPHICS] .
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Reference:
Thiazine – an overview | ScienceDirect Topics,
,Thiazine | C4H5NS – PubChem