Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mezvah A. Nobi"'
Autor:
Alexander V. Aksenov, Igor Yu. Grishin, Nicolai A. Aksenov, Vladimir V. Malyuga, Dmitrii A. Aksenov, Mezvah A. Nobi, Michael Rubin
Publikováno v:
Molecules, Vol 26, Iss 14, p 4274 (2021)
Nitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with various nucleophilic amines. Strategically placed second functionality allows for the design of annulation reactions enabling preparation of various he
Externí odkaz:
https://doaj.org/article/09587f72118e41a7ac10e904cfb9b3d7
Autor:
Alexander V. Aksenov, Elena V. Aleksandrova, Dmitrii A. Aksenov, Anna A. Aksenova, Nicolai A. Aksenov, Mezvah A. Nobi, Michael Rubin
Publikováno v:
The Journal of Organic Chemistry. 87:1434-1444
Autor:
Nicolai A. Aksenov, Alexander V. Aksenov, Lidiya A. Prityko, Dmitrii A. Aksenov, Daria S. Aksenova, Mezvah A. Nobi, Michael Rubin
Publikováno v:
ACS omega. 7(16)
A facile and highly efficient method for the preparation of 2-(3-oxoindolin-2-ylidene)acetonitriles from 4-(2-aminophenyl)-4-oxo-2-phenylbutanenitriles is described. The featured transformation operates via nucleophilic intramolecular cyclization and
Autor:
Anton A. Skomorokhov, Dmitrii A. Aksenov, Michael Rubin, Mezvah A. Nobi, Alexander V. Aksenov, Elena A. Sorokina, Nicolai A. Aksenov, Nikita K. Kirilov, Igor A. Kurenkov
Publikováno v:
RSC advances. 11(57)
The mechanistic rationale involving activation of nitroalkanes towards interaction with nucleophilic reagents in the presence of polyphosphoric acid (PPA) was re-evaluated. Could nitrile oxide moieties be formed during this process? This experiment d
Autor:
Vladimir V. Malyuga, Nicolai A. Aksenov, Dmitrii A. Aksenov, Alexander V. Aksenov, Michael Rubin, Igor Yu. Grishin, Mezvah A. Nobi
Publikováno v:
Molecules
Volume 26
Issue 14
Molecules, Vol 26, Iss 4274, p 4274 (2021)
Volume 26
Issue 14
Molecules, Vol 26, Iss 4274, p 4274 (2021)
Nitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with various nucleophilic amines. Strategically placed second functionality allows for the design of annulation reactions enabling preparation of various he