Issue 44, 2008

Rhodium(i)-catalyzed one-pot synthesis of dialkyl ketones from methanol and alkenes through directed sp3 C–H bond activation of N-methylamine

Abstract

The hydroacylation of methanol with alkenes was developed using a catalytic system consisting of Rh(I), 2-amino-4-picoline and benzoic acid; the reaction is speculated to occur by the initial N-methylation of 2-amino-4-picoline with methanol, and the subsequent dehydrogenation of the resulting N-methylamine, followed by double chelation-assisted hydroimination of alkene with the imine to give dialkyl ketones after hydrolysis.

Graphical abstract: Rhodium(i)-catalyzed one-pot synthesis of dialkyl ketones from methanol and alkenes through directed sp3 C–H bond activation of N-methylamine

Supplementary files

Article information

Article type
Communication
Submitted
15 Aug 2008
Accepted
03 Sep 2008
First published
01 Oct 2008

Chem. Commun., 2008, 5779-5781

Rhodium(I)-catalyzed one-pot synthesis of dialkyl ketones from methanol and alkenes through directed sp3 C–H bond activation of N-methylamine

E. Jo, J. Lee and C. Jun, Chem. Commun., 2008, 5779 DOI: 10.1039/B814166E

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