MICROWAVE PROMOTED PALLADIUM-CATALYZED PHENYLATION OF AROYL CHLORIDES AND SODIUM TETRAPHENYLBORATE

200111 citationsJournal Article

Authors

Jinxian Wang · Northwest Normal University

Bang‐Guo Wei · Northwest Normal University

Zhanxiang Liu · Northwest Normal University

Yihua Yang · Northwest Normal University

Abstract

A rapid and efficient method for synthesis of unsymmetrical ketones involves reaction of sodium tetraphenylborate with aroyl chlorides in the presence of catalytic amount Pd(PPh3)2Cl2 under microwave irradiation to give the corresponding phenyl ketones 3a–j in 87–98% yield.

Topics & Keywords

Chemical Synthesis and Reactions Sulfur-Based Synthesis Techniques Synthesis of Organic Compounds

UN Sustainable Development Goals

Clean water and sanitation

Publication Details

Published in: Synthetic Communications

Volume 31, Issue 24, pp. 3885-3890

DOI: 10.1081/scc-100108241

Field-Weighted Citation Impact: 1.10