Stereochemical probes of intramolecular CH insertion reactions of iron-carbene complexes

S Ishii, S Zhao, P Helquist

Index: Ishii, Shingo; Zhao, Shikai; Helquist, Paul Journal of the American Chemical Society, 2000 , vol. 122, # 24 p. 5897 - 5898

Full Text: HTML

Citation Number: 16

Abstract

A common characteristic of carbenes and metal-carbene complexes is their propensity to undergo insertion reactions into OH, NH, and CH bonds. 1 Several forms of intramolecular CH insertions, including enantioselective versions, have been developed for the construction, most importantly, of cyclopentanes and five-membered heterocycles. The importance of these reactions is reflected by their widespread use in synthesis. We have ...

Related Articles:

The Mechanism of Halide Reductions with Lithium Aluminum Hydride. IV. Tracer Studies in the Reduction of Halohydrins1

[Eliel; Prosser Journal of the American Chemical Society, 1956 , vol. 78, p. 4045,4048]

Synthesis, configuration, and optical purity of asymmetric primary alcohols

[Eliel; Delmonte Journal of the American Chemical Society, 1958 , vol. 80, p. 1744,1750]

Synthesis, configuration, and optical purity of asymmetric primary alcohols

[Eliel; Delmonte Journal of the American Chemical Society, 1958 , vol. 80, p. 1744,1750]

More Articles...