Výsledky vyhledávání - "Nadezhda V. Stoletova"

Akademický článek

Selectivity Control in Nitroaldol (Henry) Reaction by Changing the Basic Anion in a Chiral Copper(II) Complex Based on (S)-2-Aminomethylpyrrolidine and 3,5-Di-tert-butylsalicylaldehyde

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

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Synthesis and a Catalytic Study of Diastereomeric Cationic Chiral-at-Cobalt Complexes Based on (R,R)-1,2-Diphenylethylenediamine

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2c5f04a72cdbec54299bae0cb2fe7896
https://doi.org/10.1021/acs.inorgchem.1c00855

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Correction: An asymmetric metal-templated route to amino acids with an isoquinolone core via a Rh(iii)-catalyzed coupling of aryl hydroxamates with chiral propargylglycine Ni(ii) complexes

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. 21:3021-3022

Correction for ‘An asymmetric metal-templated route to amino acids with an isoquinolone core via a Rh(iii)-catalyzed coupling of aryl hydroxamates with chiral propargylglycine Ni(ii) complexes’ by Mikhail A. Arsenov et al., Org. Biomol. Chem., 20

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ff2ed89597baeaebd4b9a5e4fd809239
https://doi.org/10.1039/d3ob90047a

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An octahedral cobalt(iii) complex based on cheap 1,2-phenylenediamine as a bifunctional metal-templated hydrogen bond donor catalyst for fixation of CO2 with epoxides under ambient conditions

Autor: Michael G. Medvedev, Alexey A. Lisov, Vladimir A. Larionov, Victor I. Maleev, Alexander F. Smol'yakov, Nadezhda V. Stoletova, Mikhail A. Emelyanov

Publikováno v: Inorganic Chemistry Frontiers. 8:3871-3884

Hydrogen bond donors (HBDs) are a sustainable privileged class of catalysts which are broadly used for the activation of compounds in synthetic chemistry. Among them, the metal-templated HBD complexes present perspective systems with high catalytic p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b5cb4ac7b6103fbfce8f44fe4695af1c
https://doi.org/10.1039/d1qi00464f

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A general synthesis of unnatural α-amino acids by iron-catalysed olefin–olefin coupling via generated radicals

Autor: Nadezhda V. Stoletova, Alexander F. Smol'yakov, Tat'yana F. Savel'yeva, Vladimir A. Larionov, Vladislav I. Kovalev, Victor I. Maleev

Publikováno v: Organic Chemistry Frontiers. 6:1094-1099

Herein, we report an efficient and practical protocol for the asymmetric synthesis of unnatural α-amino acids (AAs) with γ-tertiary and quaternary carbon centres via selective intermolecular iron-catalysed olefin–olefin coupling of a chiral Ni(II

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bd932638ebe664ef4f26cd271155082b
https://doi.org/10.1039/c9qo00108e

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