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Issue 95, 2015
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Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines

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Abstract

A facile synthetic method to access 3-substituted isoquinoline or dihydroisoquinoline derivatives has been developed via a novel cyclization reaction of N-sulfonyl-1,2,3-triazole derivatives by thermally induced rearrangement.

Graphical abstract: Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines

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Supplementary files

Article information


Submitted
09 Sep 2015
Accepted
29 Sep 2015
First published
29 Sep 2015

Chem. Commun., 2015,51, 16968-16971
Article type
Communication
Author version available

Cyclization of sulfide, ether or tertiary amine-tethered N-sulfonyl-1,2,3-triazoles: a facile synthetic protocol for 3-substituted isoquinolines or dihydroisoquinolines

Y. Jiang, R. Sun, Q. Wang, X. Tang and M. Shi, Chem. Commun., 2015, 51, 16968 DOI: 10.1039/C5CC07511D

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