An article Regioselective Radical Borylation of alpha,beta-Unsaturated Esters and Related Compounds by Visible Light Irradiation with an Organic Photocatalyst WOS:000661126700051 published article about INSERTION in [Li, Guosong; Huang, Guanwang; Sun, Ruixia; Dai, Wen] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China; [Curran, Dennis P.] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15208 USA in 2021.0, Cited 28.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Application In Synthesis of Methyl 3-phenyl-2-propenoate
Radical hydroboration reactions have only recently been reported and are still rare. Here we describe a photoredox radical hydroboration of alpha,beta-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 alpha/beta regioselectivity is high. The reaction requires only the organocatalyst; there is no costly metal, and there are no other additives (base, cocatalyst, initiator).
Welcome to talk about 103-26-4, If you have any questions, you can contact Li, GS; Huang, GW; Sun, RX; Curran, DP; Dai, W or send Email.. Application In Synthesis of Methyl 3-phenyl-2-propenoate
Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
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