scispace - formally typeset
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.

Papers
More filters
Journal ArticleDOI

Novel Sequence of Two Base-Catalyzed 1,3-Proton Shifts and [1,2]-Wittig Rearrangement in the Synthesis of 2,4-Bis-(trifluoromethyl)-6-phenylpyridine.

TL;DR: In this paper, the reaction of 1.1, 1.5, 5, 5.5-hexafluoro-2,4-pentanedione with (R)-phenylglycinol was found to proceed via intermediate formation of (R, 4E, 6Z)-5, 7-bis-(trifluoromethyl)-2, 3-dihydro-3-phenyl-1, 4-oxazepine which further underwent a base-catalyzed 1,3-proton shift reaction followed by [
Journal ArticleDOI

2,2,2-Trifluoro-1-(1-adamantyl)ethylamine Hydrochloride.

TL;DR: In this paper, a convenient synthesis of a hitherto unknown fluorinated analogue of 1-(1-adamantyl)ethylamine (remantadine) starting from readily available 1-bromoadamantane and trifluoroacetic anhydride is described.
Book ChapterDOI

Synthesis of β and γ-Substituted Prolines for Conformation-Activity Relationship Studies of the α-MSH Analogue MT-II

TL;DR: This work has synthesized a series of novel, topographically constrained β and γ-substituted prolines and incorporated these optically pure substituted prolines into MT-II at positions 6 and 7.
Journal ArticleDOI

LDA-Promoted Asymmetric Synthesis of β-Trifluoromethyl-β-amino Indanone Derivatives with Virtually Complete Stereochemical Outcome.

TL;DR: In this paper, it was shown that β-trifluoromethyl-β-amino indanone derivatives can be isolated in diastereomerically pure form simply by washing the crude reaction mixture with hexanes, underscoring practicality of the present method.