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Mendeleev Communications, 2019, Volume 29, Issue 2, Pages 190–193
DOI: https://doi.org/10.1016/j.mencom.2019.03.025
(Mi mendc1467)
 

This article is cited in 4 scientific papers (total in 4 papers)

Communications

DFT and experimental study of triallylborane-mediated isomerization of α-allylated azaheterocycles

N. Yu. Kuznetsova, V. I. Malishevabc, M. G. Medvedevabd, Yu. N. Bubnovab

a A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c Higher Chemical College of the Russian Academy of Sciences, D.I. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation
d National Research University Higher School of Economics (HSE University), Moscow, Russian Federation
Abstract: Triallylborane-mediated thermal trans/cis-isomerization of α-allylated azaheterocycles is a unique stereoselective transformation providing straightforward access to important heterocycles. The main experimental features of this process, namely, thermodynamically controlled isomer ratio, 1,3-allylic strain as a driving force and regioselectivity are quantitatively described by quantum chemical calculations at B3LYP/6-31+G(d,p)/PCM(DMSO) level of theory.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (2.4 Mb)


Citation: N. Yu. Kuznetsov, V. I. Malishev, M. G. Medvedev, Yu. N. Bubnov, “DFT and experimental study of triallylborane-mediated isomerization of α-allylated azaheterocycles”, Mendeleev Commun., 29:2 (2019), 190–193
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  • https://www.mathnet.ru/eng/mendc/v29/i2/p190
  • This publication is cited in the following 4 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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