Issue 38, 2020

TfOH-promoted synthesis of 4,5-dihydrooxazolo[5,4-c]isoquinolines via formal [3 + 2] cycloaddition of 4-diazoisoquinolin-3-one and benzonitriles

Abstract

A facile and efficient method for the synthesis of novel 2-substituted 4-tosyl-4,5-dihydrooxazolo[5,4-c]isoquinolines from 4-diazoisoquinolin-3-ones and nitriles is reported. The reaction proceeded through a TfOH-promoted formal [3 + 2] cycloaddition and the products could be conveniently converted to 2-aryloxazolo[5,4-c]isoquinolines and the subsequent 2-(oxazolo[5,4-c]isoquinolin-2-yl)phenol which emitted bright green light in dilute dichloromethane solution and in solid form as well. Simple operation, metal-free and mild reaction conditions, short reaction time and broad substrate scope are the prominent features of this methodology.

Graphical abstract: TfOH-promoted synthesis of 4,5-dihydrooxazolo[5,4-c]isoquinolines via formal [3 + 2] cycloaddition of 4-diazoisoquinolin-3-one and benzonitriles

Supplementary files

Article information

Article type
Paper
Submitted
24 Aug 2020
Accepted
16 Sep 2020
First published
17 Sep 2020

Org. Biomol. Chem., 2020,18, 7671-7676

TfOH-promoted synthesis of 4,5-dihydrooxazolo[5,4-c]isoquinolines via formal [3 + 2] cycloaddition of 4-diazoisoquinolin-3-one and benzonitriles

J. Chen, Z. Li, M. Suleman, Z. Wang, P. Lu and Y. Wang, Org. Biomol. Chem., 2020, 18, 7671 DOI: 10.1039/D0OB01748E

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