An efficient palladium-catalyzed enantioselective direct -alkylation of indoles using a novel type of axially chiral styrene-phosphine ligand was developed. This reaction demonstrated good functional group compatibility and a wide range scope of substrates in mild conditions. Moreover, the DFT calculations expounded the coordination mode of the metal catalyst and the axially chiral styrene-phosphine ligand in the enantioselectivity control.
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http://dx.doi.org/10.1021/acs.joc.3c01734 | DOI Listing |
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