9 article(s) from Chebanov, Valentyn A
Multicomponent reactions IV
- Thomas J. J. Müller and
- Valentyn A. Chebanov
Beilstein J. Org. Chem. 2025, 21, 2082–2084, doi:10.3762/bjoc.21.163
Switchable pathways of multicomponent heterocyclizations of 5-amino-1,2,4-triazoles with salicylaldehydes and pyruvic acid
- Yana I. Sakhno,
- Oleksander V. Buravov,
- Kostyantyn Yu. Yurkov,
- Anastasia Yu. Andryushchenko,
- Svitlana V. Shishkina and
- Valentyn A. Chebanov
Beilstein J. Org. Chem. 2025, 21, 2030–2035, doi:10.3762/bjoc.21.158
α-Ketoglutaric acid in Ugi reactions and Ugi/aza-Wittig tandem reactions
- Vladyslav O. Honcharov,
- Yana I. Sakhno,
- Olena H. Shvets,
- Vyacheslav E. Saraev,
- Svitlana V. Shishkina,
- Tetyana V. Shcherbakova and
- Valentyn A. Chebanov
Beilstein J. Org. Chem. 2025, 21, 2021–2029, doi:10.3762/bjoc.21.157
Ugi bisamides based on pyrrolyl-β-chlorovinylaldehyde and their unusual transformations
- Alexander V. Tsygankov,
- Vladyslav O. Vereshchak,
- Tetiana O. Savluk,
- Serhiy M. Desenko,
- Valeriia V. Ananieva,
- Oleksandr V. Buravov,
- Yana I. Sakhno,
- Svitlana V. Shishkina and
- Valentyn A. Chebanov
Beilstein J. Org. Chem. 2024, 20, 1773–1784, doi:10.3762/bjoc.20.156
Synthesis of imidazo[1,2-a]pyridine-containing peptidomimetics by tandem of Groebke–Blackburn–Bienaymé and Ugi reactions
- Oleksandr V. Kolomiiets,
- Alexander V. Tsygankov,
- Maryna N. Kornet,
- Aleksander A. Brazhko,
- Vladimir I. Musatov and
- Valentyn A. Chebanov
Beilstein J. Org. Chem. 2023, 19, 727–735, doi:10.3762/bjoc.19.53
Effective microwave-assisted approach to 1,2,3-triazolobenzodiazepinones via tandem Ugi reaction/catalyst-free intramolecular azide–alkyne cycloaddition
- Maryna O. Mazur,
- Oleksii S. Zhelavskyi,
- Eugene M. Zviagin,
- Svitlana V. Shishkina,
- Vladimir I. Musatov,
- Maksim A. Kolosov,
- Elena H. Shvets,
- Anna Yu. Andryushchenko and
- Valentyn A. Chebanov
Beilstein J. Org. Chem. 2021, 17, 678–687, doi:10.3762/bjoc.17.57
Ultrasonic-assisted unusual four-component synthesis of 7-azolylamino-4,5,6,7-tetrahydroazolo[1,5-a]pyrimidines
- Yana I. Sakhno,
- Maryna V. Murlykina,
- Oleksandr I. Zbruyev,
- Anton V. Kozyryev,
- Svetlana V. Shishkina,
- Dmytro Sysoiev,
- Vladimir I. Musatov,
- Sergey M. Desenko and
- Valentyn A. Chebanov
Beilstein J. Org. Chem. 2020, 16, 281–289, doi:10.3762/bjoc.16.27
In water multicomponent synthesis of low-molecular-mass 4,7-dihydrotetrazolo[1,5-a]pyrimidines
- Irina G. Tkachenko,
- Sergey A. Komykhov,
- Vladimir I. Musatov,
- Svitlana V. Shishkina,
- Viktoriya V. Dyakonenko,
- Vladimir N. Shvets,
- Mikhail V. Diachkov,
- Valentyn A. Chebanov and
- Sergey M. Desenko
Beilstein J. Org. Chem. 2019, 15, 2390–2397, doi:10.3762/bjoc.15.231
Doebner-type pyrazolopyridine carboxylic acids in an Ugi four-component reaction
- Maryna V. Murlykina,
- Oleksandr V. Kolomiets,
- Maryna M. Kornet,
- Yana I. Sakhno,
- Sergey M. Desenko,
- Victoriya V. Dyakonenko,
- Svetlana V. Shishkina,
- Oleksandr A. Brazhko,
- Vladimir I. Musatov,
- Alexander V. Tsygankov,
- Erik V. Van der Eycken and
- Valentyn A. Chebanov
Beilstein J. Org. Chem. 2019, 15, 1281–1288, doi:10.3762/bjoc.15.126
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