Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Victor I, Maleev"'
Autor:
Olga V. Khromova, Lidiya V. Yashkina, Nadezhda V. Stoletova, Victor I. Maleev, Yuri N. Belokon, Vladimir A. Larionov
Publikováno v:
Molecules, Vol 29, Iss 21, p 5207 (2024)
This article is a continuation of our previous research on the catalytic capability of a chiral copper complex based on commercially available (S)-2-aminomethylpyrrolidine and 3,5-di-tert-butylsalicylaldehyde with various counter-anions in the asymme
Externí odkaz:
https://doaj.org/article/33686dc481ec4a339791f1094bd72ac7
Autor:
Hegine I. Hakobyan, Silva M. Jamgaryan, Armen S. Sargsyan, Yuri M. Danghyan, Vladimir A. Larionov, Victor I. Maleev, Ashot S. Saghyan, Zorayr Z. Mardiyan
Publikováno v:
Symmetry, Vol 15, Iss 10, p 1924 (2023)
Nowadays, amino acids (AAs) and peptides with bulky side chains hold significant interest for organic synthesis and the modern pharma industry. Non-proteinogenic (or unnatural) AAs are key building blocks used for obtaining pharmaceutically relevant
Externí odkaz:
https://doaj.org/article/23f0ee5434b2475cb4704d456a54306f
Autor:
Anna S. Tovmasyan, Anna F. Mkrtchyan, Hamlet N. Khachatryan, Mary V. Hayrapetyan, Robert M. Hakobyan, Artavazd S. Poghosyan, Avetis H. Tsaturyan, Ela V. Minasyan, Victor I. Maleev, Vladimir A. Larionov, Armen G. Ayvazyan, Norio Shibata, Giovanni N. Roviello, Ashot S. Saghyan
Publikováno v:
Molecules, Vol 28, Iss 3, p 1180 (2023)
A new family of Cu(II) and Ni(II) salen complexes was synthesized and fully characterized through various physicochemical methods. Their catalytic activity was evaluated in the phase transfer Cα-alkylation reaction of the Schiff bases of D,L-alanine
Externí odkaz:
https://doaj.org/article/5b90462ad04541998c0eda0dba8608ed
Autor:
Zalina T. Gugkaeva, Zorayr Z. Mardiyan, Alexander F. Smol’yakov, Artavazd S. Poghosyan, Ashot S. Saghyan, Victor I. Maleev, Vladimir A. Larionov
Publikováno v:
Organic Letters. 24:6230-6235
A practically useful protocol for the asymmetric synthesis of artificial β-aryl-substituted cysteine derivatives was developed through sequential Pd(II)-catalyzed Heck cross-coupling with aryl iodides and hydrothiolation reaction with various alkyl
Autor:
Zalina T. Gugkaeva, Maria V. Panova, Alexander F. Smol'yakov, Michael G. Medvedev, Alan T. Tsaloev, Ivan A. Godovikov, Victor I. Maleev, Vladimir A. Larionov
Publikováno v:
Advanced Synthesis & Catalysis. 364:2395-2402
Autor:
Olga V. Khromova, Mikhail A. Emelyanov, Alexander F. Smol’yakov, Ivan V. Fedyanin, Victor I. Maleev, Vladimir A. Larionov
Publikováno v:
Inorganic Chemistry. 61:5512-5523
A family of well-defined Λ- and Δ-diastereomeric octahedral cationic chiral-at-cobalt complexes were obtained by a simple two-step reaction of (
Autor:
Mikhail A. Arsenov, Nadezhda V. Stoletova, Tat'yana F. Savel'yeva, Alexander F. Smol'yakov, Victor I. Maleev, Dmitry A. Loginov, Vladimir A. Larionov
Publikováno v:
Organic & Biomolecular Chemistry. 20:9385-9391
The first asymmetric route to artificial amino acids with an isoquinolone skeleton was elaborated via a straightforward Rh(iii)-catalyzed C–H activation/annulation reaction.
Autor:
Olga V. Khromova, Mikhail A. Emelyanov, Nadezhda V. Stoletova, Ekaterina E. Bodunova, Darya O. Prima, Alexander F. Smol’yakov, Igor L. Eremenko, Victor I. Maleev, Vladimir A. Larionov
Publikováno v:
Organometallics.
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1614-1623 (2015)
Two new one-component aluminium-based catalysts for the reaction between epoxides and carbon dioxide have been prepared. The catalysts are composed of aluminium–salen chloride complexes with trialkylammonium groups directly attached to the aromatic
Externí odkaz:
https://doaj.org/article/6cfd5759a3ee4deabe7bb762286aa97a
Autor:
Alexander F. Smol'yakov, Mikhail M. Il’in, Mikhail A. Emelyanov, Vladimir A. Larionov, Victor I. Maleev, Nadezhda V. Stoletova
Publikováno v:
Inorganic Chemistry. 60:13960-13967
Here we report the first synthesis of two diastereomeric cationic octahedral Co(III) complexes based on commercially available (R,R)-1,2-diphenylethylenediamine and salicylaldehyde. Both diastereoisomers with opposite chiralities at the metal center