Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 7-Day Trial for You or Your Team.

Learn More →

Ruthenium‐Catalyzed Regioselective α‐Alkylation of Ketones: The First Alkyl‐Group Transfer from Trialkylamines to the α‐C Atom of Ketones

Ruthenium‐Catalyzed Regioselective α‐Alkylation of Ketones: The First Alkyl‐Group Transfer from... A new reaction: A ruthenium‐catalyzed transfer of an alkyl group from a trialkylamine to the α‐carbon atom of a ketone leads in good yields to α‐alkylated ketones (Eq. (1)). The reaction is applicable to a wide range of alkyl(alkyl), alkyl(aryl), and cyclic ketones, and in the case of unsymmetrical ketones it takes place regioselectively at the less hindered α‐position. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Angewandte Chemie International Edition Wiley

Ruthenium‐Catalyzed Regioselective α‐Alkylation of Ketones: The First Alkyl‐Group Transfer from Trialkylamines to the α‐C Atom of Ketones

Loading next page...
 
/lp/wiley/ruthenium-catalyzed-regioselective-alkylation-of-ketones-the-first-0ugPUHhs2f

References (27)

Publisher
Wiley
Copyright
Copyright © 2001 Wiley Subscription Services
ISSN
1433-7851
eISSN
1521-3773
DOI
10.1002/1521-3773(20010302)40:5<958::AID-ANIE958>3.0.CO;2-4
Publisher site
See Article on Publisher Site

Abstract

A new reaction: A ruthenium‐catalyzed transfer of an alkyl group from a trialkylamine to the α‐carbon atom of a ketone leads in good yields to α‐alkylated ketones (Eq. (1)). The reaction is applicable to a wide range of alkyl(alkyl), alkyl(aryl), and cyclic ketones, and in the case of unsymmetrical ketones it takes place regioselectively at the less hindered α‐position.

Journal

Angewandte Chemie International EditionWiley

Published: Jan 2, 2001

Keywords: ; ; ; ;

There are no references for this article.