A. Tsaloev

发表

Using the same organocatalyst for asymmetric synthesis of both enantiomers of glutamic acid-derived Ni(II) complexes via 1,4-additions of achiral glycine and dehydroalanine Schiff base Ni(II) complexes

Y. Belokon’, V. Khrustalev, V. I. Maleev, 2012, Amino Acids.

Four hydroxyls are better than two. The use of a chiral lithium salt of 3,3′-bis-methanol-2,2′-binaphthol as a multifunctional catalyst of enantioselective Michael addition reactions

Y. Belokon’, V. Khrustalev, V. I. Maleev, 2011 .

Asymmetric opening of styrene oxide with p-toluidine catalyzed by BINOL polyols and their lithium complexes

Y. Belokon’, A. Peregudov, V. I. Maleev, 2013, Russian Chemical Bulletin.

New bifunctional organocatalysts based on (R,R)-cyclohexane-1,2-diamine for the asymmetric addition of nucleophiles to aldehydes

V. Khrustalev, V. I. Maleev, V. Khrustalev, 2012, Russian Chemical Bulletin.

Tetraaryl-1,3-dioxolane-4,5-dimethanols as catalysts for the addition of trimethylsilyl cyanide to benzaldehyde and the oxirane ring

K. Lyssenko, Y. Belokon’, V. Khrustalev, 2007 .

A mechanistic study of the Lewis acid–Brønsted base–Brønsted acid catalysed asymmetric Michael addition of diethyl malonate to cyclohexenone

M. North, K. Lyssenko, Y. Belokon’, 2017 .

Bis-TADDOLs as bifunctional organocatalysts for trifluoromethylation of aldehydes and ring-opening of cyclohexene oxide with p-toluidine

M. North, Y. Belokon’, V. I. Maleev, 2010 .

Economical Synthesis of α-Amino Acids from a Novel Family of Easily Available Schiff Bases of Glycine Esters and 2-Hydroxybenzophenone

Y. Nelyubina, Y. Belokon’, V. Khrustalev, 2017, Synthesis.

Cyclic products of the Ugi reaction of aldehydo and keto carboxylic acids: chemoselective modification

S. Tkachenko, M. Krasavin, A. Ivachtchenko, 2011 .

Asymmetric Metal‐Templated Route to Amino Acids with 3‐Spiropyrrolidine Oxindole Core via a 1,3‐Dipolar Addition of Azomethine Ylides to a Chiral Dehydroalanine Ni(II) Complex

I. Godovikov, A. Smolyakov, Z. Gugkaeva, 2022, Advanced Synthesis & Catalysis.