Issue 26, 2017

Convenient preparation of 4-diazoisochroman-3-imines and 3-subsituted 3,5-dihydroisochromeno[3,4-d][1,2,3]triazoles

Abstract

A novel and convenient preparation of 4-diazoisochroman-3-imines through the copper(I)-catalyzed cascade reaction of (2-ethynylphenyl)-methanols with sulfonyl azides is described. The synthesized cyclical α-diazo imidates could readily react with a variety of primary amines to furnish 3-substituted 3,5-dihydroisochromeno[3,4-d][1,2,3]-triazoles under catalyst-free conditions.

Graphical abstract: Convenient preparation of 4-diazoisochroman-3-imines and 3-subsituted 3,5-dihydroisochromeno[3,4-d][1,2,3]triazoles

Supplementary files

Article information

Article type
Communication
Submitted
22 Jan 2017
Accepted
13 Mar 2017
First published
13 Mar 2017

Chem. Commun., 2017,53, 3769-3772

Convenient preparation of 4-diazoisochroman-3-imines and 3-subsituted 3,5-dihydroisochromeno[3,4-d][1,2,3]triazoles

A. Ren, P. Lu and Y. Wang, Chem. Commun., 2017, 53, 3769 DOI: 10.1039/C7CC00603A

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