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Russian Chemical Reviews, 2014, Volume 83, Issue 6, Pages 475–501
DOI: https://doi.org/10.1070/RC2014v083n06ABEH004418 (Mi rcr699) 		 
This article is cited in 32 scientific papers (total in 32 papers)

C-Ethynylpyrroles: synthesis and reactivity

L. N. Sobenina, D. N. Tomilin, B. A. Trofimov

A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
English full-text Citations (32)
DOI: https://doi.org/10.1070/RC2014v083n06ABEH004418
Abstract: The principal methods for the synthesis of C-ethynylpyrroles are presented. The mechanisms of reactions underlying these methods are considered. The reactivity of C-ethynylpyrroles is discussed with primary attention being given to cycloaddition and intramolecular cyclization involving the ethynyl substituent, resulting in new pyrrole systems.
Bibliography — 131 references.
Received: 08.07.2013
Russian version:
Uspekhi Khimii, 2014, Volume 83, Issue 6, Pages 475–501
DOI: https://doi.org/10.1070/RC2014v083n06ABEH004418
Bibliographic databases:
Language: English
Original paper language: Russian
Citation: L. N. Sobenina, D. N. Tomilin, B. A. Trofimov, “C-Ethynylpyrroles: synthesis and reactivity”, Usp. Khim., 83:6 (2014), 475–501; Russian Chem. Reviews, 83:6 (2014), 475–501
Citation in format AMSBIB
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\paper C-Ethynylpyrroles: synthesis and reactivity
\jour Usp. Khim.
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\vol 83
\issue 6
\pages 475--501
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\crossref{https://doi.org/10.1070/RC2014v083n06ABEH004418}
\elib{https://elibrary.ru/item.asp?id=21818592}
\transl
\jour Russian Chem. Reviews
\yr 2014
\vol 83
\issue 6
\pages 475--501
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  • https://doi.org/10.1070/RC2014v083n06ABEH004418
  • https://www.mathnet.ru/eng/rcr/v83/i6/p475
    • This publication is cited in the following 32 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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