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Mendeleev Communications, 2016, Volume 26, Issue 6, Pages 500–501
DOI: https://doi.org/10.1016/j.mencom.2016.11.013
(Mi mendc2259)
 

This article is cited in 5 scientific papers (total in 5 papers)

Communications

HUSY zeolite promoted hydrophenylation of alkynes conjugated with electron-withdrawing substituents

D. S. Ryabukhinab, A. V. Vasilyevab

a St. Petersburg State Forest Tecnical University, St. Petersburg, Russian Federation
b Institute of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation
Abstract: Arylacetylenes, conjugated with electron-withdrawing groups, ArC≡C(EWG) [EWG = SO2Ph, PO(OEt)2, COMe, CO2Me] in reaction with benzene at room temperature or 130°C (glass high pressure tube) for 1–10h under the action of acidic zeolite HUSY (Si /Al ratio is 15) afford products of hydrophenylation of acetylene bond Ar(Ph)C=CH(EWG) in yields of 56–98%.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (877.9 Kb)


Citation: D. S. Ryabukhin, A. V. Vasilyev, “HUSY zeolite promoted hydrophenylation of alkynes conjugated with electron-withdrawing substituents”, Mendeleev Commun., 26:6 (2016), 500–501
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  • https://www.mathnet.ru/eng/mendc/v26/i6/p500
  • This publication is cited in the following 5 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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