Regiospecific synthesis of N2-aryl 1,2,3-triazoles from 2,5-disubstituted tetrazoles via photochemically generated nitrile imine intermediates
Stewart, Sam and Harris, Robert and Jamieson, Craig (2014) Regiospecific synthesis of N2-aryl 1,2,3-triazoles from 2,5-disubstituted tetrazoles via photochemically generated nitrile imine intermediates. Synlett, 25 (17). pp. 2480-2484. ISSN 0936-5214
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Official URL: https://doi.org/10.1055/s-0034-1379010
Abstract
The synthesis of N2-aryl 1,2,3-triazoles from 2,5-disubstituted tetrazoles was achieved under photochemical conditions. This simple and mild one-step reaction provides regiospecific access to 2,4,5-substituted 1,2,3-triazoles via a nitrile imine intermediate. Syntheses of alkyl and heterocylic derivatives were also investigated.
Creators(s): |
Stewart, Sam ![]() ![]() | Item type: | Article |
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ID code: | 51137 |
Keywords: | photochemistry, regioselectivity, tetrazole, triazole, indazole, Chemistry, Organic Chemistry |
Subjects: | Science > Chemistry |
Department: | Faculty of Science > Pure and Applied Chemistry |
Depositing user: | Pure Administrator |
Date deposited: | 16 Jan 2015 14:53 |
Last modified: | 20 Jan 2021 21:45 |
Related URLs: | |
URI: | https://strathprints.strath.ac.uk/id/eprint/51137 |
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