An article Vicinal Diboration of Alkyl Bromides via Tandem Catalysis WOS:000471212100090 published article about ALKYLBORONIC ESTERS; BOND FORMATION; BORYLATION; SECONDARY; SUBSTITUTION; CONSTRUCTION; ACTIVATION; ALKENES; HALIDES in [Wang, Xiao-Xu; Li, Lei; Gong, Tian Jun; Xiao, Bin; Lu, Xi; Fuo, Yao] Univ Sci & Technol China, iChEM, Anhui Prov Key Lab Biomass Clean Energy, Hefei Natl Lab Phys Sci Microscale,CAS Key Lab Ur, Hefei 230026, Anhui, Peoples R China in 2019.0, Cited 62.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3. Recommanded Product: 103-25-3
Vicinal diboration of alkyl bromides via tandem catalysis is reported. The reported reaction exhibits a broad substrate scope, good functional group compatibility, and regioselectivity. Moreover, it shows good practicality due to the easy accessibility of alkyl bromides in combination with diverse transformations of diboronates. Mechanism study indicates that terminal alkenes are generated selectively through nickel-catalyzed dehydrohalogenation of alkyl bromides followed by base/MeOH promoted diboration process to provide 1,2-diboration products.
Recommanded Product: 103-25-3. About Methyl 3-phenylpropionate, If you have any questions, you can contact Wang, XX; Li, L; Gong, TJ; Xiao, B; Lu, X; Fuo, Y or concate me.
Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics