Issue 91, 2019

An unexpected coupling–reduction tandem reaction for the synthesis of alkenyl-substituted BODIPYs

Abstract

We report an unexpected coupling–reduction tandem reaction as a general and efficient one-pot synthesis of alkenyl-substituted boron dipyrromethene (BODIPY) from chlorinated-BODIPY and alkyne. This unique synthesis combined the Sonogashira coupling reaction and reduction reaction without adding an additional reagent, which shows higher yields, broader substrate scope and faster reaction rate compared with the conventional methods of the Knoevenagel reaction and Heck coupling reaction.

Graphical abstract: An unexpected coupling–reduction tandem reaction for the synthesis of alkenyl-substituted BODIPYs

Supplementary files

Article information

Article type
Communication
Submitted
02 Oct 2019
Accepted
22 Oct 2019
First published
22 Oct 2019

Chem. Commun., 2019,55, 13761-13764

An unexpected coupling–reduction tandem reaction for the synthesis of alkenyl-substituted BODIPYs

K. Teng, L. Niu, J. Li, L. Jia and Q. Yang, Chem. Commun., 2019, 55, 13761 DOI: 10.1039/C9CC07730H

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