V
Vadim A. Soloshonok
Researcher at University of the Basque Country
Publications - 417
Citations - 16252
Vadim A. Soloshonok is an academic researcher from University of the Basque Country. The author has contributed to research in topics: Enantioselective synthesis & Amino acid. The author has an hindex of 64, co-authored 406 publications receiving 14170 citations. Previous affiliations of Vadim A. Soloshonok include University of Oklahoma & Centre national de la recherche scientifique.
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Journal Article
Aktivatsiia 5-lipoksigenazy lipofil'nymi n-alkilsoderzhashchimi kislotami--allostericheskiǐ protsess.
TL;DR: Mechanism of the activation of 5-lipoxygenase (EC 1.13.11.12) has been investigated and shown to have the allosteric character andLimitations of the activator structure are formulated.
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Asymmetric Synthesis of Phosphorus Analogues of Dicarboxylic α- Amino Acids.
Vadim A. Soloshonok,Yu. N. Belokon,N. A. Kuz'mina,V. I. Maleev,N. Yu. Svistunova,V. A. Solodenko,V. P. Kukhar +6 more
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Asymmetric Synthesis of Fluorine‐Containing Amines, Amino Alcohols, α‐ and β‐Amino Acids Mediated by Chiral Sulfinyl Group
TL;DR: In this article, a review article provides a critical overview of several different synthetic approaches developed for asymmetric preparation of fluorine-containing amines, amino alcohols, α- and β-amino acids.
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Asymmetric synthesis of (S)-α-(octyl)glycine via alkylation of Ni(II) complex of chiral glycine Schiff base.
Bo Fu,Ryosuke Takeda,Yupiao Zou,Hiroyuki Konno,Hiroki Moriwaki,Hidenori Abe,Jianlin Han,Kunisuke Izawa,Vadim A. Soloshonok +8 more
TL;DR: Under the optimized conditions, the alkylation proceeds with excellent yield and diastereoselectivity and the observed stereochemical outcome and convenient reaction conditions bode well for application of this method for large-scale asymmetric synthesis of (S)-2-aminodecanoic acid and its derivatives.
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Asymmetric synthesis of (S)-3-methyleneglutamic acid and its N-Fmoc derivative via Michael addition-elimination reaction of chiral glycine Ni (II) complex with enol tosylates.
Yuhei Shigeno,Jianlin Han,Vadim A. Soloshonok,Vadim A. Soloshonok,Hiroki Moriwaki,Wataru Fujiwara,Hiroyuki Konno +6 more
TL;DR: In this paper, the first example of enantioselective preparation of (S)-3-methyleneglutamic acid and its N-Fmoc derivative via a new type of Michael addition-elimination reaction between chiral nucleophilic glycine equivalent and enol tosylates was reported.