Issue 39, 2016

Ruthenium-catalyzed direct α-alkylation of amides using alcohols

Abstract

The highly efficient direct α-alkylation of unactivated amides has been accomplished using alcohols in the presence of the Ru-PNN catalyst (0.1 mol%) with a high turnover number. Using this approach, 2-oxindole was directly transformed into C3-alkylated 3-hydroxyindolin-2-one in one step without the use of any oxidant.

Graphical abstract: Ruthenium-catalyzed direct α-alkylation of amides using alcohols

Supplementary files

Article information

Article type
Communication
Submitted
16 Aug 2016
Accepted
09 Sep 2016
First published
09 Sep 2016

Org. Biomol. Chem., 2016,14, 9215-9220

Ruthenium-catalyzed direct α-alkylation of amides using alcohols

M. B. Chaudhari, G. S. Bisht, P. Kumari and B. Gnanaprakasam, Org. Biomol. Chem., 2016, 14, 9215 DOI: 10.1039/C6OB01786J

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