An article Lewis acid-promoted site-selective cyanation of phenols WOS:000544927100013 published article about C-H CYANATION; PALLADIUM-CATALYZED CYANATION; ELECTROPHILIC CYANATION; MEDIATED CYANATION; PRACTICAL METHOD; ARYL HALIDES; ACETONITRILE; ARENES; TRANSFORMATION; DERIVATIVES in [Zhang, Wu; Yang, Wen; Zhao, Wanxiang] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometries, Changsha 410082, Hunan, Peoples R China in 2020.0, Cited 66.0. Category: indole-building-block. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6
An efficient Lewis acid-promoted site-selective electrophilic cyanation of 3-substituted and 3,4-disubstituted phenols has been developed. The cyanation reactions using MeSCN as the cyanating reagent proceeded efficiently to afford a wide range of 2-hydroxybenzonitriles with high efficiency and excellent regioselectivity. This protocol could provide a practical method for the synthesis and modification of biologically active molecules.
Category: indole-building-block. Welcome to talk about 150-19-6, If you have any questions, you can contact Zhang, W; Yang, W; Zhao, WX or send Email.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles