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Mendeleev Communications, 2020, Volume 30, Issue 4, Pages 494–495
DOI: https://doi.org/10.1016/j.mencom.2020.07.029
(Mi mendc1234)
 

This article is cited in 3 scientific papers (total in 3 papers)

Communications

Unusual multiple insertion of diazo carbonyl compounds into (purin-6-yl)benzene derivative

M. M. Vinogradova, D. V. Vorobyevaa, Yu. V. Nelyubinaa, S. N. Osipovab, D. A. Loginovac

a A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
b Moscow Region State Pedagogical University, Mytishi, Moscow Region, Russian Federation
c G.V. Plekhanov Russian University of Economics, Moscow, Russian Federation
Abstract: The consecutive alkylation of 9-isopropyl-6-phenyl-9H-purine with methyl 2-diazo-3,3,3-trifluoropropionate and diethyl diazomalonate proceeds at the phenyl substituent firstly via ortho-C–H activation under chelation-assistance of the purine core, followed by classical electrophilic metal carbenoid insertion to the C−H bond of a malonate moiety.
Keywords: carbenoids, C–H functionalization, diazo compounds, organofluorine compounds, homogeneous catalysis, nitrogen heterocycles, purines.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.1 Mb)


Citation: M. M. Vinogradov, D. V. Vorobyeva, Yu. V. Nelyubina, S. N. Osipov, D. A. Loginov, “Unusual multiple insertion of diazo carbonyl compounds into (purin-6-yl)benzene derivative”, Mendeleev Commun., 30:4 (2020), 494–495
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  • https://www.mathnet.ru/eng/mendc/v30/i4/p494
  • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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