Arylation of Aldehydes To Directly Form Ketones via Tandem Nickel Catalysis
Tandem
Stereocenter
DOI:
10.1021/acs.orglett.9b01782
Publication Date:
2019-07-16T18:12:56Z
AUTHORS (4)
ABSTRACT
A nickel-catalyzed arylation of both aliphatic and aromatic aldehydes proceeds with air-stable (hetero)arylboronic acids, an exceptionally wide substrate scope. The neutral condition tolerates acidic hydrogen sensitive polar groups also preserves α-stereocenters some chiral aldehydes. Interestingly, this nickel(0) catalysis does not follow common 1,2-insertion arylmetal species to β-hydrogen elimination.
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