Simplifying nickel (0) catalysis: an air-stable nickel precatalyst for the internally selective benzylation of terminal alkenes

EA Standley, TF Jamison

Index: Standley, Eric A.; Jamison, Timothy F. Journal of the American Chemical Society, 2013 , vol. 135, # 4 p. 1585 - 1592

Full Text: HTML

Citation Number: 53

Abstract

The synthesis and characterization of the air-stable nickel (II) complex trans-(PCy2Ph) 2Ni (o- tolyl) Cl is described in conjunction with an investigation of its use for the Mizoroki–Heck- type, room temperature, internally selective coupling of substituted benzyl chlorides with terminal alkenes. This reaction, which employs a terminal alkene as an alkenylmetal equivalent, provides rapid, convergent access to substituted allylbenzene derivatives in ...

Related Articles:

A Carbon-14 Tracer Study of the Alkaline Rearrangement of Chlorophenanthraquinones1, 2

[Ott; Smith Journal of the American Chemical Society, 1955 , vol. 77, p. 2325,2328]

Acetolysis reactivities of substituted benzyl and polycyclic arylmethyl p-toluenesulfonates. Correlations with SCF [self-consistant field]-. pi. and CNDO [complete …

[Streitwieser,A. et al. Journal of the American Chemical Society, 1970 , vol. 92, # 17 p. 5141 - 5150]

More Articles...