On June 4, 2021, Li, Guosong; Huang, Guanwang; Sun, Ruixia; Curran, Dennis P.; Dai, Wen published an article.Recommanded Product: 6197-30-4 The title of the article was Regioselective Radical Borylation of α,β-Unsaturated Esters and Related Compounds by Visible Light Irradiation with an Organic Photocatalyst. And the article contained the following:
Radical hydroboration reactions have only recently been reported and are still rare. Here the authors describe a photoredox radical hydroboration of α,β-unsaturated esters, amides, ketones, and nitriles with NHC-boranes that uses only an organocatalyst and visible light. The conditions are mild, the substrate scope is broad, and the α/β regioselectivity is high. The reaction requires only the organocatalyst; there is no costly metal, and there are no other additives (base, cocatalyst, initiator). The experimental process involved the reaction of 2-Ethylhexyl 2-cyano-3,3-diphenylacrylate(cas: 6197-30-4).Recommanded Product: 6197-30-4
The Article related to unsaturated ester amide nitrile regioselective photochem radical borylation organocatalyst, boryl ester amide nitrile preparation, Organometallic and Organometalloidal Compounds: Boron Compounds and other aspects.Recommanded Product: 6197-30-4
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics