Recently I am researching about BONDS; ACTIVATION; AMINATION; FUNCTIONALIZATION, Saw an article supported by the NIHUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) – USA [R01 GM126832, R35 GM134929, 1S10 OD020022-1]; Ruth L. Kirschstein NRSA fellowshipUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) – USA [F32 GM129909]; NSFNational Science Foundation (NSF) [CHE-1048642]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Vasilopoulos, A; Golden, DL; Buss, JA; Stahl, SS. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate. Formula: C10H12O2
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.
Formula: C10H12O2. 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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