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Mendeleev Communications, 2016, Volume 26, Issue 1, Pages 3–5
DOI: https://doi.org/10.1016/j.mencom.2016.01.002
(Mi mendc2089)
 

This article is cited in 8 scientific papers (total in 8 papers)

Communications

Stereoselective one-pot synthesis of (1Z)- and (1E)-1-arylmethylidene-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazoles by cyclization of alk-4-ynals with o-diaminobenzene

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

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (200 kB) Citations (8)
Abstract: Cyclization of alk-4-ynals with o-diaminobenzene in DMSO under the sequential action of NH4Br and base (KOH or K2CO3) affords 1-arylmethylidene-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazoles, which are formed selectively as E- or Z-isomers depending on the base used.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (353.9 Kb)


Citation: V. D. Gvozdev, K. N. Shavrin, M. P. Egorov, O. M. Nefedov, “Stereoselective one-pot synthesis of (1Z)- and (1E)-1-arylmethylidene-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazoles by cyclization of alk-4-ynals with o-diaminobenzene”, Mendeleev Commun., 26:1 (2016), 3–5
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  • https://www.mathnet.ru/eng/mendc/v26/i1/p3
  • This publication is cited in the following 8 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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