TY - JOUR
T1 - Graphene-Catalyzed Direct Friedel-Crafts Alkylation Reactions
T2 - Mechanism, Selectivity, and Synthetic Utility
AU - Hu, Feng
AU - Patel, Mehulkumar
AU - Luo, Feixiang
AU - Flach, Carol
AU - Mendelsohn, Richard
AU - Garfunkel, Eric
AU - He, Huixin
AU - Szostak, Michal
N1 - Publisher Copyright:
© 2015 American Chemical Society.
PY - 2015/10/23
Y1 - 2015/10/23
N2 - Transition-metal-catalyzed alkylation reactions of arenes have become a central transformation in organic synthesis. Herein, we report the first general strategy for alkylation of arenes with styrenes and alcohols catalyzed by carbon-based materials, exploiting the unique property of graphenes to produce valuable diarylalkane products in high yields and excellent regioselectivity. The protocol is characterized by a wide substrate scope and excellent functional group tolerance. Notably, this process constitutes the first general application of graphenes to promote direct C-C bond formation utilizing polar functional groups anchored on the GO surface, thus opening the door for an array of functional group alkylations using benign and readily available graphene materials. Mechanistic studies suggest that the reaction proceeds via a tandem catalysis mechanism in which both of the coupling partners are activated by interaction with the GO surface.
AB - Transition-metal-catalyzed alkylation reactions of arenes have become a central transformation in organic synthesis. Herein, we report the first general strategy for alkylation of arenes with styrenes and alcohols catalyzed by carbon-based materials, exploiting the unique property of graphenes to produce valuable diarylalkane products in high yields and excellent regioselectivity. The protocol is characterized by a wide substrate scope and excellent functional group tolerance. Notably, this process constitutes the first general application of graphenes to promote direct C-C bond formation utilizing polar functional groups anchored on the GO surface, thus opening the door for an array of functional group alkylations using benign and readily available graphene materials. Mechanistic studies suggest that the reaction proceeds via a tandem catalysis mechanism in which both of the coupling partners are activated by interaction with the GO surface.
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U2 - 10.1021/jacs.5b09636
DO - 10.1021/jacs.5b09636
M3 - Article
AN - SCOPUS:84947761170
VL - 137
SP - 14473
EP - 14480
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 45
ER -