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Mendeleev Communications, 2017, Volume 27, Issue 2, Pages 178–179
DOI: https://doi.org/10.1016/j.mencom.2017.03.024 (Mi mendc1936) 		 
This article is cited in 10 scientific papers (total in 10 papers)

Communications

Synthesis of 3-(5-chloropyrazol-3-yl)propenals

A. V. Popov, V. A. Kobelevskaya, L. I. Larina, G. G. Levkovskaya

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
Full-text PDF (200 kB) Citations (10) Supplementary materials
DOI: https://doi.org/10.1016/j.mencom.2017.03.024
Abstract: The Vielsmeier–Haack formylation of 5-chloro-3-alkenylpyrazoles proceeds at the olefinic double bond and affords (2E)-3-(5-chloro-1H-pyrazol-3-yl)prop-2-enals.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.2 Mb)


Citation: A. V. Popov, V. A. Kobelevskaya, L. I. Larina, G. G. Levkovskaya, “Synthesis of 3-(5-chloropyrazol-3-yl)propenals”, Mendeleev Commun., 27:2 (2017), 178–179
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    • This publication is cited in the following 10 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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