4.4 Article

Direct conversion of aromatic ketones to arenecarboxylic esters via carbon-carbon bond-cleavage reactions

Journal

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN
Volume 81, Issue 3, Pages 369-372

Publisher

CHEMICAL SOC JAPAN
DOI: 10.1246/bcsj.81.369

Keywords

-

Ask authors/readers for more resources

Aromatic methyl ketones, P-keto esters, and trifluoromethyl-1,3-diketones can be directly converted to arenecarboxylic esters via carbon-carbon bond cleavage of pyridinium iodide intermediates in the presence of copper(II) oxide, iodine, pyridine, and potassium carbonate in alcoholic media. The advantages of the present method in terms of good yields, mild reaction conditions, and inexpensive reagents should make this protocol a valuable alternative to the existing methods.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available