Issue 70, 2016

Highly enantioselective construction of carbazole derivatives via [4+2] cycloaddition of silyloxyvinylindoles and β,γ-unsaturated α-ketoesters

Abstract

A highly efficient catalytic asymmetric [4+2] cycloaddition of silyloxyvinylindoles with β,γ-unsaturated α-ketoesters has been accomplished by an available chiral N,N′-dioxide/yttrium triflate complex. A widespread range of carbazole derivatives were obtained in 47–98% yield with 86–99% ee under mild reaction conditions.

Graphical abstract: Highly enantioselective construction of carbazole derivatives via [4+2] cycloaddition of silyloxyvinylindoles and β,γ-unsaturated α-ketoesters

Supplementary files

Article information

Article type
Communication
Submitted
27 Jun 2016
Accepted
01 Aug 2016
First published
02 Aug 2016

Chem. Commun., 2016,52, 10692-10695

Highly enantioselective construction of carbazole derivatives via [4+2] cycloaddition of silyloxyvinylindoles and β,γ-unsaturated α-ketoesters

X. Zhao, H. Mei, Q. Xiong, K. Fu, L. Lin, X. Liu and X. Feng, Chem. Commun., 2016, 52, 10692 DOI: 10.1039/C6CC05328A

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