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Vitaliy N. Chernenko
Institution:
State Scientific Institution “Institute for Single Crystals” of National Academy of Sciences of Ukraine
Observed institutions:
National Academy of Sciences of Ukraine,
University of Graz,
University of Konstanz,
State Scientific Institution “Institute for Single Crystals” of National Academy of Sciences of Ukraine,
Technical University of Munich
OpenAlex ID:
A5110121773
Tuning of Chemo- and Regioselectivities in Multicomponent Condensations of 5-Aminopyrazoles, Dimedone, and Aldehydes
2008
·
Valentin A. Chebanov
, Vyacheslav E. Saraev
, et al.
·
The Journal of Organic Chemistry
·
176
One-Pot, Multicomponent Route to Pyrazoloquinolizinones
2007
·
Valentin A. Chebanov
, Vyacheslav E. Saraev
, et al.
·
Organic Letters
·
81
Cyclocondensation reactions of 5-aminopyrazoles, pyruvic acids and aldehydes. Multicomponent approaches to pyrazolopyridines and related products
2006
·
Valentin A. Chebanov
, Yana I. Sakhno
, et al.
·
Tetrahedron
·
79
Green and efficient synthesis of pyrazolo[3,4‐b]quinolin‐5‐ones derivatives by microwave‐assisted multicomponent reaction in hot water medium
2010
·
Anastasiya Yu. Andriushchenko
, Sergey M. Desenko
, et al.
·
Journal of Heterocyclic Chemistry
·
32
ChemInform Abstract: Green and Efficient Synthesis of Pyrazolo[3,4‐b]quinolin‐5‐ones Derivatives by Microwave‐Assisted Multicomponent Reaction in Hot Water Medium.
2011
·
Anastasiya Yu. Andriushchenko
, Sergey M. Desenko
, et al.
·
ChemInform
ChemInform Abstract: Tuning of Chemo‐ and Regioselectivities in Multicomponent Condensations of 5‐Aminopyrazoles, Dimedone, and Aldehydes.
2008
·
Valentin A. Chebanov
, Vyacheslav E. Saraev
, et al.
·
ChemInform
One‐Pot, Multicomponent Route to Pyrazoloquinolizinones.
2007
·
Valentin A. Chebanov
, Vyacheslav E. Saraev
, et al.
·
ChemInform
Cyclocondensation Reactions of 5‐Aminopyrazoles, Pyruvic Acids and Aldehydes. Multicomponent Approaches to Pyrazolopyridines and Related Products.
2007
·
Valentin A. Chebanov
, Yana I. Sakhno
, et al.
·
ChemInform
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Works count:
8
Citation count:
368
H-index:
4
I10-index:
4
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