Vadim A.
Soloshonok
National Institute of Advanced Industrial Science and Technology
Tsukuba, JapónPublicaciones en colaboración con investigadores/as de National Institute of Advanced Industrial Science and Technology (35)
2015
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Carbonyl group coordination preferences in square-planar NiII and PdII complexes of pentadentate ligands by electron-withdrawing/donating substituents
Inorganica Chimica Acta, Vol. 433, pp. 3-12
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Introducing a new radical trifluoromethylation reagent
Chemical Communications, Vol. 51, Núm. 27, pp. 5967-5970
2014
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Substituent-controlled preference of carbonyl group-metal coordination in d8 metal complexes with non-symmetric pentadentate ligands. Structural and stereochemical aspects
Dalton Transactions, Vol. 43, Núm. 14, pp. 5375-5381
2013
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Optical purifications via self-disproportionation of enantiomers by achiral chromatography: Case study of a series of α-CF3-containing secondary alcohols
Chirality, Vol. 25, Núm. 6, pp. 365-368
2011
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Biomimetic transamination - a metal-free alternative to the reductive amination. Application for generalized preparation of fluorine-containing amines and amino acids
Current Organic Synthesis, Vol. 8, Núm. 2, pp. 281-294
2010
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Biomimetic reductive amination under the continuous-flow reaction conditions
Journal of Fluorine Chemistry, Vol. 131, Núm. 2, pp. 261-265
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First principle lattice energy calculations for enantiopure and racemic crystals of α-(trifluoromethyl)lactic acid: Is self-disproportionation of enantiomers controlled by thermodynamic stability of crystals?
Journal of Fluorine Chemistry, Vol. 131, Núm. 4, pp. 461-466
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Ridge-tile-like chiral topology: Synthesis, resolution, and complete chiroptical characterization of enantiomers of edge-sharing binuclear square planar complexes of Ni(II) bearing achiral ligands
Journal of the American Chemical Society, Vol. 132, Núm. 30, pp. 10477-10483
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Self-disproportionation of enantiomers of isopropyl 3,3,3-(trifluoro)lactate via sublimation: Sublimation rates vs. enantiomeric composition
Journal of Fluorine Chemistry, Vol. 131, Núm. 4, pp. 535-539
2009
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Continuous-flow asymmetric biomimetic transamination
Journal of Fluorine Chemistry, Vol. 130, Núm. 5, pp. 512-515
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Operationally convenient asymmetric synthesis of (S)-2-amino-3,3-bis-(4-fluorophenyl)propanoic acid
Journal of Fluorine Chemistry, Vol. 130, Núm. 6, pp. 547-549
2008
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First example of continuous-flow reaction conditions for biomimetic reductive amination of fluorine-containing carbonyl compounds
Journal of Fluorine Chemistry, Vol. 129, Núm. 9, pp. 785-787
2003
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Convenient asymmetric synthesis of, β-substituted α,α -difluoro-β-amino acids via reformatsky reaction between Davis' N-sulfinylimines and ethyl bromodifluoroacetate
Journal of Organic Chemistry, Vol. 68, Núm. 19, pp. 7448-7454
1999
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Asymmetric synthesis of α-arylglycinols via additions of lithium methyl p-tolyl sulfoxide to N-(PMP)arylaldimines followed by 'non oxidative' Pummerer reaction
Tetrahedron, Vol. 55, Núm. 10, pp. 3025-3040
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Biomimetic, reducing agent-free reductive amination of fluorocarbonyl compounds: Practical asymmetric synthesis of enantiopure fluoroamines and amino acids
ACS Symposium Series, Vol. 746, pp. 74-83
1998
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Biomimetic Transamination of α-Alkyl β-Keto Carboxylic Esters. Chemoenzymatic Approach to the Stereochemically Defined α-Alkyl β-Fluoroalkyl β-Amino Acids
Journal of Organic Chemistry, Vol. 63, Núm. 6, pp. 1878-1884
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Chiral sulfoxide controlled asymmetric additions to C-N double bond. An efficient approach to stereochemically defined α-fluoroalkyl amino compounds
Tetrahedron, Vol. 54, Núm. 42, pp. 12789-12806
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Highly diastereoselective methylene transfer from diazomethane to the carbonyl of β-keto sulfoxides. A general approach to synthetically versatile fluorine-containing chiral building blocks
Tetrahedron, Vol. 54, Núm. 39, pp. 11841-11860
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Synthesis and reactivity of enantiomerically pure 2-fluoromethyl-2-(1'- p-tolylsulfinyl) alkyl oxiranes
Tetrahedron, Vol. 54, Núm. 39, pp. 11825-11840
1997
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An efficient asymmetric synthesis of (2S,3S)-3-trifluoromethylproglutamic acid
Tetrahedron Letters, Vol. 38, Núm. 27, pp. 4903-4904