Safety of Methyl 3-phenylpropionate. In 2020.0 ORG LETT published article about BONDS; ACTIVATION; AMINATION; FUNCTIONALIZATION in [Vasilopoulos, Aristidis; Golden, Dung L.; Buss, Joshua A.; Stahl, Shannon S.] Univ Wisconsin, Dept Chem, 1101 Univ Ave, Madison, WI 53706 USA in 2020.0, Cited 46.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3.
Site-selective transformation of benzylic C-H bonds into diverse functional groups is achieved via Cu-catalyzed C-H fluorination with N-fluorobenzenesulfonimide (NFSI), followed by substitution of the resulting fluoride with various nucleophiles. The benzyl fluorides generated in these reactions are reactive electrophiles in the presence of hydrogen-bond donors or Lewis acids, allowing them to be used without isolation in C-O, C-N, and C-C coupling reactions.
Safety of Methyl 3-phenylpropionate. About Methyl 3-phenylpropionate, If you have any questions, you can contact Vasilopoulos, A; Golden, DL; Buss, JA; Stahl, SS or concate me.
Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
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