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.
Original language | English |
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Pages (from-to) | 79385-79390 |
Number of pages | 6 |
Journal | RSC Advances |
Volume | 5 |
Issue number | 97 |
DOIs | |
State | Published - 14 Sep 2015 |
Bibliographical note
Publisher Copyright:© The Royal Society of Chemistry 2015.