Issue 1, 2020

Rhodium-catalyzed homodimerization–cyclization reaction of two vinyl isocyanides: a general route to 2-(isoquinolin-1-yl)oxazoles

Abstract

A novel rhodium-catalyzed homodimerization–cyclization reaction of two vinyl isocyanides has been developed for the first time. In this reaction, the highly reactive 1,4-diazabutatriene intermediates generated by the homodimerization of two vinyl isocyanides could undergo a novel type of intramolecular tandem cyclization and provides a new and highly efficient method for the construction of 2-(isoquinolin-1-yl)oxazoles by formation of three new bonds and two rings from readily available acyclic starting materials in a single step.

Graphical abstract: Rhodium-catalyzed homodimerization–cyclization reaction of two vinyl isocyanides: a general route to 2-(isoquinolin-1-yl)oxazoles

Supplementary files

Article information

Article type
Research Article
Submitted
08 Oct 2019
Accepted
21 Nov 2019
First published
22 Nov 2019

Org. Chem. Front., 2020,7, 126-130

Rhodium-catalyzed homodimerization–cyclization reaction of two vinyl isocyanides: a general route to 2-(isoquinolin-1-yl)oxazoles

Z. Wang, X. Meng, P. Liu, W. Hu and Y. Zhao, Org. Chem. Front., 2020, 7, 126 DOI: 10.1039/C9QO01229J

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