Issue 88, 2013

Ni-Catalyzed [8+3] cycloaddition of tropones with 1,1-cyclopropanediesters

Abstract

A variety of cycloheptapyrane derivatives were prepared via Ni-catalyzed formal [8+3] cycloaddition of tropones with 1,1-cyclopropanediesters. The asymmetric version of the process can be achieved using either an enantiomerically enriched cyclopropane as the starting material or a racemic cyclopropane and a chiral Lewis acid.

Graphical abstract: Ni-Catalyzed [8+3] cycloaddition of tropones with 1,1-cyclopropanediesters

Supplementary files

Article information

Article type
Communication
Submitted
22 Jul 2013
Accepted
11 Sep 2013
First published
17 Sep 2013

Chem. Commun., 2013,49, 10406-10408

Ni-Catalyzed [8+3] cycloaddition of tropones with 1,1-cyclopropanediesters

R. Tejero, A. Ponce, J. Adrio and J. C. Carretero, Chem. Commun., 2013, 49, 10406 DOI: 10.1039/C3CC45552A

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