Issue 97, 2015

Synthesis of ketones via organolithium addition to acid chlorides using continuous flow chemistry

Abstract

An efficient method for the synthesis of ketones using organolithium and acid chlorides under continuous flow conditions has been developed. In contrast to standard batch chemistry, over-addition of the organolithium to the ketone for the formation of the undesired tertiary alcohol has been minimised representing a direct approach toward ketones.

Graphical abstract: Synthesis of ketones via organolithium addition to acid chlorides using continuous flow chemistry

Supplementary files

Article information

Article type
Communication
Submitted
27 Jul 2015
Accepted
14 Sep 2015
First published
14 Sep 2015

RSC Adv., 2015,5, 79385-79390

Author version available

Synthesis of ketones via organolithium addition to acid chlorides using continuous flow chemistry

S. Moon, S. Jung, U. Bin Kim and W. Kim, RSC Adv., 2015, 5, 79385 DOI: 10.1039/C5RA14890A

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