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Mendeleev Communications, 2002, Volume 12, Issue 6, Pages 224–225
DOI: https://doi.org/10.1070/MC2002v012n06ABEH001703 (Mi mendc4173) 		 
This article is cited in 7 scientific papers (total in 7 papers)

Alk-1-ynyl(3-pyridyl)- and alk-1-ynyl(2-thienyl)carbenes as the first example of (alk-1-ynyl)carbenes with hetaryl substituents at carbenic centres

K. N. Shavrin, V. D. Gvozdev, O. M. Nefedov

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (81 kB) Citations (7)
DOI: https://doi.org/10.1070/MC2002v012n06ABEH001703
Abstract: Alk-1-ynyl(hetaryl)carbenes 3 have been generated from 1-(tosyloxy)-1-hetarylalk-2-ynes 2 via the elimination of para-toluenesulfonic acid on the treatment with ButOK.
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Document Type: Article
Language: English


Citation: K. N. Shavrin, V. D. Gvozdev, O. M. Nefedov, “Alk-1-ynyl(3-pyridyl)- and alk-1-ynyl(2-thienyl)carbenes as the first example of (alk-1-ynyl)carbenes with hetaryl substituents at carbenic centres”, Mendeleev Commun., 12:6 (2002), 224–225
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  • https://www.mathnet.ru/eng/mendc/v12/i6/p224
    • This publication is cited in the following 7 articles:
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