Issue 19, 2019

Cobalt-catalyzed cyclization with the introduction of cyano, acyl and aminoalkyl groups

Abstract

An efficient synthesis of carbo- and heterocycles using C[double bond, length as m-dash]C, C[double bond, length as m-dash]O and C[double bond, length as m-dash]N bonds under cobalt catalysis is described. The substituents on olefins are key for controlling the regio- and chemoselectivity in the initial hydrogen atom transfer step and quaternary carbons are efficiently constructed under mild conditions. Cyclopropane cleavage and tandem cyclization give highly functionalized bicyclic skeletons in a single operation.

Graphical abstract: Cobalt-catalyzed cyclization with the introduction of cyano, acyl and aminoalkyl groups

Supplementary files

Article information

Article type
Paper
Submitted
19 Mar 2019
Accepted
18 Apr 2019
First published
22 Apr 2019

Org. Biomol. Chem., 2019,17, 4783-4788

Cobalt-catalyzed cyclization with the introduction of cyano, acyl and aminoalkyl groups

H. Hori, S. Arai and A. Nishida, Org. Biomol. Chem., 2019, 17, 4783 DOI: 10.1039/C9OB00637K

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