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Mendeleev Communications, 1999, Volume 9, Issue 1, Pages 5–7
DOI: https://doi.org/10.1070/MC1999v009n01ABEH001060
(Mi mendc4501)
 

This article is cited in 6 scientific papers (total in 6 papers)

Intriguing modes of addition of 1,3,4-triphenyl-4,5-dihydro-1H-1,2,4-triazol- 5-ylidene to bicyclopropylidene

A. de Meijerea, S. I. Kozhushkova, D. S. Yufitb, J. A. Howardb

a Institut für Organische Chemie der Georg-August-Universität Göttingen, Göttingen, Germany
b Department of Chemistry, University of Durham, Durham, UK
Full-text PDF (259 kB) Citations (6)
Abstract: 1,3,4-Triphenyl-4,5-dihydro-1H-1,2,4-triazol-5-ylidene 1 reacts with bicyclopropylidene 2 to yield four unexpected products 3–6, none of which resembles the typical [2+1] mode of cycloaddition observed for 1 with electron-deficient alkenes.
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Document Type: Article
Language: English


Citation: A. de Meijere, S. I. Kozhushkov, D. S. Yufit, J. A. Howard, “Intriguing modes of addition of 1,3,4-triphenyl-4,5-dihydro-1H-1,2,4-triazol- 5-ylidene to bicyclopropylidene”, Mendeleev Commun., 9:1 (1999), 5–7
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  • This publication is cited in the following 6 articles:
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