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 ArticleDOI
Asymmetric synthesis of (1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid by sequential SN2–SN2′ dialkylation of (R)-N-(benzyl)proline-derived glycine Schiff base Ni(II) complex
Aki Kawashima,Chen Xie,Haibo Mei,Ryosuke Takeda,Akie Kawamura,Tatsunori Sato,Hiroki Moriwaki,Kunisuke Izawa,Jianlin Han,José Luis Aceña,Vadim A. Soloshonok,Vadim A. Soloshonok +11 more
TL;DR: In this article, a new process for the asymmetric synthesis of (1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid of high pharmaceutical importance is described.
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Enantiomeric Enrichments via the Self-Disproportionation of Enantiomers (SDE) by Achiral, Gravity-Driven Column Chromatography: a Case Study Using N-(1-Phenylethyl)acetamide for Optimizing the Enantiomerically Pure Yield and Magnitude of the SDE
Alicja Wzorek,Azusa Sato,Józef Drabowicz,Józef Drabowicz,Vadim A. Soloshonok,Vadim A. Soloshonok,Karel D. Klika +6 more
TL;DR: In this paper, the authors explored the self-disproportionation of enantiomers via achiral, gravity-driven column chromatography for enantiomeric enrichment using N-(1-phenylethyl)acetamide (PEA).
Journal ArticleDOI
Asymmetric synthesis of novel sterically constrained amino acids
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Development of Hamari Ligands for Practical Asymmetric Synthesis of Tailor-Made Amino Acids
Jianlin Han,Todd T. Romoff,Hiroki Moriwaki,Hiroyuki Konno,Vadim A. Soloshonok,Vadim A. Soloshonok +5 more
TL;DR: A brief summary of the development of axially chiral tridentate Hamari ligands and their application for general asymmetric synthesis of various structural types of amino acids is provided.
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Large-scale Mannich-type reactions of (SS)-N-tert-butanesulfinyl-(3,3,3)-trifluoroacetaldimine with C-nucleophiles
TL;DR: In this paper, the first attempts to scale up five addition reactions between (SS)-N-tert-butanesulfinyl-(3, 3,3,3)-trifluoroacetaldimine 6 with C-nucleophiles derived from ketones were described.