Harrington, Ross and Stanforth, Stephen (2012) The unexpected conversion of a thiophene ring into a pyrrole ring via a putative nitrene intermediate. Tetrahedron Letters, 53 (16). pp. 2111-2113. ISSN 0040-4039
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Official URL: http://dx.doi.org/10.1016/j.tetlet.2012.02.050
Abstract
Triethylphosphite induced reductive cyclisation of 1-(2-nitrophenyl)-3,5-di(2-thienyl)pyrazole 6 afforded the expected 1,3-di(2-thienyl)pyrazolo[1,2-a]benzotriazole 7 (14%) together with an unexpected product which was shown to be a 2-(2-thienyl)pyrazolo[1,5-a]pyrrolo[2,1-c]quinoxaline 8 derivative (27%). A mechanism for the extrusion of sulfur during the transformation of heterocycle 6 into product 8 is proposed.
Item Type: | Article |
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Uncontrolled Keywords: | Heterocyclic mesomeric betaines, reductive cyclisation, nitrenes, Pyrazolo[1,2-a]benzotriazole, Pyrazolo[1,5-a]pyrrolo[2,1-c]quinoxaline, thiophenes, polythiophenes |
Subjects: | F100 Chemistry |
Department: | Faculties > Health and Life Sciences > Applied Sciences |
Depositing User: | Ellen Cole |
Date Deposited: | 17 Dec 2012 10:31 |
Last Modified: | 12 Oct 2019 18:27 |
URI: | http://nrl.northumbria.ac.uk/id/eprint/10642 |
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