Issue 48, 2014

Highly enantioselective reaction of 2-oxindoles with (3-indolyl)methanols by cooperative Catalysis of a Lewis acid and organocatalyst

Abstract

An efficient cooperative biscinchona alkaloid and Lewis acid catalytic system was developed in the enantioselective α-alkylation of 2-oxindoles with (3-indolyl)(phenyl)methanols to provide (2-oxindole)-linker-indole derivatives in good yields (70–83%) with high enantioselectivities (81%–92%).

Graphical abstract: Highly enantioselective reaction of 2-oxindoles with (3-indolyl)methanols by cooperative Catalysis of a Lewis acid and organocatalyst

Supplementary files

Article information

Article type
Paper
Submitted
24 Sep 2014
Accepted
13 Oct 2014
First published
13 Oct 2014

Org. Biomol. Chem., 2014,12, 9881-9886

Highly enantioselective reaction of 2-oxindoles with (3-indolyl)methanols by cooperative Catalysis of a Lewis acid and organocatalyst

C. Ren, T. Zhang, X. Wang, T. Wu, J. Ma, Q. Xuan, F. Wei, H. Huang, D. Wang and L. Liu, Org. Biomol. Chem., 2014, 12, 9881 DOI: 10.1039/C4OB02035A

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