Asymmetric Friedel-Crafts alkylation of indoles with β-nitrostyrenes catalyzed by a chiral N<sup>II</sup> complex based on (<em>S</em>)-(2-aminomethyl)pyrrolidine and 3,5-di-<em>tert</em>-butylsalicylaldehyde

μ-(Acetato)nickel(II) complex with Schiff base of (<em>S</em>)-(2-aminomethyl)pyrrolidine and 3,5-di-<em>tert</em>-butyl-2-hydroxybenzaldehyde as the chiral ligand was tested in the asymmetric Friedel-Crafts alk</em>ylation of indoles with β-nitrostyrenes. The reactions catalyzed by 5 mol

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Journal
Mendeleev Communications
Published
2025-01-01
DOI
https://doi.org/10.71267/mencom.7701
Primary Topic
Synthesis of Indole Derivatives
Type
article
Field-Weighted Citation Impact
0.00

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article

Asymmetric Friedel-Crafts alkylation of indoles with β-nitrostyrenes catalyzed by a chiral NII complex based on (S)-(2-aminomethyl)pyrrolidine and 3,5-di-tert-butylsalicylaldehyde

Nadezhda V. Stoletova, Vladimir A. Larionov, Victor I. Maleev, Evgeniy V. Rozhkov et al.
Mendeleev Communications
Synthesis of Indole Derivatives
article

Asymmetric Friedel-Crafts alkylation of indoles with β-nitrostyrenes catalyzed by a chiral NII complex based on (S)-(2-aminomethyl)pyrrolidine and 3,5-di-tert-butylsalicylaldehyde

Nadezhda V. Stoletova, Vladimir A. Larionov, Victor I. Maleev, Evgeniy V. Rozhkov, Alexander V. Bachinskiy, Jr Ilyin Mikhail Mikhailovich
article en

Abstract

μ-(Acetato)nickel(II) complex with Schiff base of (<em>S</em>)-(2-aminomethyl)pyrrolidine and 3,5-di-<em>tert</em>-butyl-2-hydroxybenzaldehyde as the chiral ligand was tested in the asymmetric Friedel-Crafts alk</em>ylation of indoles with β-nitrostyrenes. The reactions catalyzed by 5 mol

Mendeleev CommunicationsVol. 35(4)
Russian Academy of Sciences (RU), D. Mendeleyev University of Chemical Technology of Russia (RU), A. N. Nesmeyanov Institute of Organoelement Compounds (RU)
Russian Science Foundation
Openalex Percentile: Top 92%
Synthesis of Indole Derivatives
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