Issue 23, 2010

Chiral Brønsted acid catalyzed asymmetric Friedel–Crafts alkylation reaction of indoles with α,β-unsaturated ketones: short access to optically active 2- and 3-substituted indole derivatives

Abstract

The asymmetric Friedel–Crafts alkylation reaction of indoles with α,β-unsaturated ketones catalyzed by chiral phosphoric acid is reported. A wide range of indoles and 4,7-dihydroindoles were allowed to react with α,β-unsaturated ketones to give the corresponding 1,4-adducts in good to high chemical yields and with excellent enantioselectivities.

Graphical abstract: Chiral Brønsted acid catalyzed asymmetric Friedel–Crafts alkylation reaction of indoles with α,β-unsaturated ketones: short access to optically active 2- and 3-substituted indole derivatives

Article information

Article type
Paper
Submitted
02 Jun 2010
Accepted
06 Aug 2010
First published
28 Sep 2010

Org. Biomol. Chem., 2010,8, 5448-5454

Chiral Brønsted acid catalyzed asymmetric Friedel–Crafts alkylation reaction of indoles with α,β-unsaturated ketones: short access to optically active 2- and 3-substituted indole derivatives

T. Sakamoto, J. Itoh, K. Mori and T. Akiyama, Org. Biomol. Chem., 2010, 8, 5448 DOI: 10.1039/C0OB00197J

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