Vadim A. Soloshonok - Publications

Affiliations: 
Department of Chemistry and Biochemistry University of Oklahoma, Norman, OK, United States 
Area:
Organic Chemistry

39 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Xie C, Zhang L, Sha W, Soloshonok VA, Han J, Pan Y. Detrifluoroacetylative in Situ Generation of Free 3-Fluoroindolin-2-one-Derived Tertiary Enolates: Design, Synthesis, and Assessment of Reactivity toward Asymmetric Mannich Reactions. Organic Letters. PMID 27305459 DOI: 10.1021/acs.orglett.6b01516  1
2016 Nian Y, Wang J, Zhou S, Dai W, Wang S, Moriwaki H, Kawashima A, Soloshonok VA, Liu H. Purely Chemical Approach for Preparation of D-alpha-amino Acids via (S)-to-(R)-interconversion of Unprotected Tailor-made alpha-amino Acids. The Journal of Organic Chemistry. PMID 27053152 DOI: 10.1021/acs.joc.5b02707  1
2016 Xie C, Zhang L, Mei H, Pajkert R, Ponomarenko M, Pan Y, Röschenthaler GV, Soloshonok VA, Han J. New Chiral Reagent for Installation of Pharmacophoric (S)- or (R)-2-(Alkoxyphosphono)-1-Amino-2,2-Difluoroethyl Group. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26952046 DOI: 10.1002/chem.201600758  1
2016 Zhou Y, Wang J, Gu Z, Wang S, Zhu W, Aceña JL, Soloshonok VA, Izawa K, Liu H. Next Generation of Fluorine-Containing Pharmaceuticals, Compounds Currently in Phase II-III Clinical Trials of Major Pharmaceutical Companies: New Structural Trends and Therapeutic Areas. Chemical Reviews. PMID 26756377 DOI: 10.1021/acs.chemrev.5b00392  1
2016 Wzorek A, Sato A, Drabowicz J, Soloshonok VA, Klika KD. Remarkable magnitude of the self-disproportionation of enantiomers (SDE) via achiral chromatography: application to the practical-scale enantiopurification of β-amino acid esters. Amino Acids. 48: 605-13. PMID 26704565 DOI: 10.1007/s00726-015-2152-5  1
2015 Kawashima A, Shu S, Takeda R, Kawamura A, Sato T, Moriwaki H, Wang J, Izawa K, Aceña JL, Soloshonok VA, Liu H. Advanced asymmetric synthesis of (1R,2S)-1-amino-2-vinylcyclopropanecarboxylic acid by alkylation/cyclization of newly designed axially chiral Ni(II) complex of glycine Schiff base. Amino Acids. PMID 26661034 DOI: 10.1007/s00726-015-2138-3  1
2015 Li T, Zhou S, Wang J, Aceña JL, Soloshonok VA, Liu H. Asymmetric synthesis of (2S,3S)-alpha-(1-oxoisoindolin-3-yl)glycines under low-basicity "kinetic" control. The Journal of Organic Chemistry. PMID 26523334 DOI: 10.1021/acs.joc.5b01730  1
2015 Nian Y, Wang J, Zhou S, Wang S, Moriwaki H, Kawashima A, Soloshonok VA, Liu H. Recyclable Ligands for the Non-Enzymatic Dynamic Kinetic Resolution of Challenging α-Amino Acids. Angewandte Chemie (International Ed. in English). PMID 26367134 DOI: 10.1002/anie.201507273  1
2015 Wang S, Zhou S, Wang J, Nian Y, Kawashima A, Moriwaki H, Aceña JL, Soloshonok VA, Liu H. Chemical Dynamic Thermodynamic Resolution and S/R Interconversion of Unprotected Unnatural Tailor-Made alpha-Amino Acids. The Journal of Organic Chemistry. PMID 26352915 DOI: 10.1021/acs.joc.5b01292  1
2015 Sato A, Han J, Ono T, Wzorek A, Aceña JL, Soloshonok VA. Introducing a new radical trifluoromethylation reagent. Chemical Communications (Cambridge, England). 51: 5967-70. PMID 25736068 DOI: 10.1039/c5cc00905g  0.36
2015 Li T, Zhou S, Wang J, Aceña JL, Soloshonok VA, Liu H. Asymmetric synthesis of α-(1-oxoisoindolin-3-yl)glycine: Synthetic and mechanistic challenges Chemical Communications. 51: 1624-1626. PMID 25500794 DOI: 10.1039/c4cc05659k  1
2014 Takeda R, Kawamura A, Kawashima A, Sato T, Moriwaki H, Izawa K, Akaji K, Wang S, Liu H, Aceña JL, Soloshonok VA. Chemical dynamic kinetic resolution and S/R interconversion of unprotected α-amino acids. Angewandte Chemie (International Ed. in English). 53: 12214-7. PMID 25244328 DOI: 10.1002/anie.201407944  1
2014 Qian P, Xie C, Wu L, Mei H, Soloshonok VA, Han J, Pan Y. Asymmetric synthesis of (3S,1′S)-3-(1-amino-2,2,2-trifluoroethyl)-1-(alkyl)-indolin-2-one derivatives by addition of (S)-N-t-butylsulfinyl-3,3,3-trifluoroacetaldimine to 1-(alkyl)-indolin-2-ones Organic and Biomolecular Chemistry. 12: 7909-7913. PMID 25220306 DOI: 10.1039/c4ob01453g  1
2014 Takeda R, Kawamura A, Kawashima A, Moriwaki H, Sato T, Aceña JL, Soloshonok VA. Design and synthesis of (S)- and (R)-α-(phenyl)ethylamine-derived NH-type ligands and their application for the chemical resolution of α-amino acids. Organic & Biomolecular Chemistry. 12: 6239-49. PMID 25008025 DOI: 10.1039/c4ob00669k  1
2014 Moriwaki H, Resch D, Li H, Ojima I, Takeda R, Aceña JL, Soloshonok VA. Synthesis and stereochemical assignments of diastereomeric Ni(II) complexes of glycine Schiff base with (R)-2-(N-{2-[N-alkyl-N-(1-phenylethyl)amino]acetyl}amino)benzophenone; a case of configurationally stable stereogenic nitrogen. Beilstein Journal of Organic Chemistry. 10: 442-8. PMID 24605164 DOI: 10.3762/bjoc.10.41  1
2014 Han J, Ono T, Uekusa H, Klika KD, Soloshonok VA. Substituent-controlled preference of carbonyl group-metal coordination in d8 metal complexes with non-symmetric pentadentate ligands. Structural and stereochemical aspects. Dalton Transactions (Cambridge, England : 2003). 43: 5375-81. PMID 24519315 DOI: 10.1039/c3dt53312c  0.36
2014 Shibata N, Nishimine T, Shibata N, Tokunaga E, Kawada K, Kagawa T, Aceña JL, Sorochinsky AE, Soloshonok VA. Asymmetric Mannich reaction between (S)-N-(tert-butanesulfinyl)-3,3,3-trifluoroacetaldimine and malonic acid derivatives. Stereodivergent synthesis of (R)- and (S)-3-amino-4,4,4-trifluorobutanoic acids. Organic & Biomolecular Chemistry. 12: 1454-62. PMID 24445698 DOI: 10.1039/c3ob42425a  1
2014 Bergagnini M, Fukushi K, Han J, Shibata N, Roussel C, Ellis TK, Aceña JL, Soloshonok VA. NH-type of chiral Ni(II) complexes of glycine Schiff base: design, structural evaluation, reactivity and synthetic applications. Organic & Biomolecular Chemistry. 12: 1278-91. PMID 24424805 DOI: 10.1039/c3ob41959b  1
2013 Sorochinsky AE, Katagiri T, Ono T, Wzorek A, Aceña JL, Soloshonok VA. Optical purifications via self-disproportionation of enantiomers by achiral chromatography: case study of a series of α-CF3-containing secondary alcohols. Chirality. 25: 365-8. PMID 23716267 DOI: 10.1002/chir.22180  0.36
2013 Wang J, Liu H, Aceña JL, Houck D, Takeda R, Moriwaki H, Sato T, Soloshonok VA. Synthesis of bis-α,α'-amino acids through diastereoselective bis-alkylations of chiral Ni(II)-complexes of glycine. Organic & Biomolecular Chemistry. 11: 4508-15. PMID 23715131 DOI: 10.1039/c3ob40594j  1
2013 Sorochinsky AE, Ueki H, Aceña JL, Ellis TK, Moriwaki H, Sato T, Soloshonok VA. Chemical approach for interconversion of (S)- and (R)-α-amino acids. Organic & Biomolecular Chemistry. 11: 4503-7. PMID 23715058 DOI: 10.1039/c3ob40541a  1
2012 Soloshonok VA, Aceña JL, Ueki H, Han J. Design and synthesis of quasi-diastereomeric molecules with unchanging central, regenerating axial and switchable helical chirality via cleavage and formation of Ni(II)-O and Ni(II)-N coordination bonds. Beilstein Journal of Organic Chemistry. 8: 1920-8. PMID 23209532 DOI: 10.3762/bjoc.8.223  0.52
2010 Soloshonok VA, Ono T, Ueki H, Vanthuyne N, Balaban TS, Bürck J, Fliegl H, Klopper W, Naubron JV, Bui TT, Drake AF, Roussel C. 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. 132: 10477-83. PMID 20662525 DOI: 10.1021/ja103296g  0.52
2009 Soloshonok VA, Ellis TK, Ueki H, Ono T. Resolution/deracemization of chiral alpha-amino acids using resolving reagents with flexible stereogenic centers. Journal of the American Chemical Society. 131: 7208-9. PMID 19422236 DOI: 10.1021/ja9026055  1
2009 Ueki H, Soloshonok VA. New sterically driven mode for generation of helical chirality. Organic Letters. 11: 1797-800. PMID 19354321 DOI: 10.1021/ol900357d  0.52
2007 Soloshonok VA, Ueki H, Yasumoto M, Mekala S, Hirschi JS, Singleton DA. Phenomenon of optical self-purification of chiral non-racemic compounds. Journal of the American Chemical Society. 129: 12112-3. PMID 17850147 DOI: 10.1021/ja065603a  1
2007 Soloshonok VA, Ueki H, Moore JL, Ellis TK. Design and synthesis of molecules with switchable chirality via formation and cleavage of metal-ligand coordination bonds. Journal of the American Chemical Society. 129: 3512-3. PMID 17338523 DOI: 10.1021/ja067995r  1
2007 Soloshonok VA, Ueki H. Design, synthesis, and characterization of binuclear Ni(II) complexes with inherent helical chirality. Journal of the American Chemical Society. 129: 2426-7. PMID 17286404 DOI: 10.1021/ja0671215  0.52
2006 Yamada T, Okada T, Sakaguchi K, Ohfune Y, Ueki H, Soloshonok VA. Efficient asymmetric synthesis of novel 4-substituted and configurationally stable analogues of thalidomide. Organic Letters. 8: 5625-8. PMID 17107088 DOI: 10.1021/ol0623668  0.52
2006 Ellis TK, Ueki H, Yamada T, Ohfune Y, Soloshonok VA. Design, synthesis, and evaluation of a new generation of modular nucleophilic glycine equivalents for the efficient synthesis of sterically constrained alpha-amino acids. The Journal of Organic Chemistry. 71: 8572-8. PMID 17064036 DOI: 10.1021/jo0616198  1
2005 Soloshonok VA, Cai C, Yamada T, Ueki H, Ohfune Y, Hruby VJ. Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of beta-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity. Journal of the American Chemical Society. 127: 15296-303. PMID 16248672 DOI: 10.1021/ja0535561  1
2004 Soloshonok VA, Ueki H, Tiwari R, Cai C, Hruby VJ. Virtually complete control of simple and face diastereoselectivity in the Michael addition reactions between achiral equivalents of a nucleophilic glycine and (S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: practical method for preparation of beta-substituted pyroglutamic acids and prolines. The Journal of Organic Chemistry. 69: 4984-90. PMID 15255725 DOI: 10.1021/jo0495438  1
2003 Sorochinsky A, Voloshin N, Markovsky A, Belik M, Yasuda N, Uekusa H, Ono T, Berbasov DO, Soloshonok VA. Convenient asymmetric synthesis of beta-substituted alpha,alpha-difluoro-beta-amino acids via Reformatsky reaction between Davis' N-sulfinylimines and ethyl bromodifluoroacetate. The Journal of Organic Chemistry. 68: 7448-54. PMID 12968899 DOI: 10.1021/jo030082k  1
2003 Ueki H, Ellis TK, Martin CH, Boettiger TU, Bolene SB, Soloshonok VA. Improved synthesis of proline-derived Ni(II) complexes of glycine: versatile chiral equivalents of nucleophilic glycine for general asymmetric synthesis of alpha-amino acids. The Journal of Organic Chemistry. 68: 7104-7. PMID 12946159 DOI: 10.1021/jo0301494  1
2003 Ellis TK, Martin CH, Tsai GM, Ueki H, Soloshonok VA. Efficient synthesis of serically constrained smmetrically alpha,alpha-disubstituted alpha-amino acids under operationally convenient conditions. The Journal of Organic Chemistry. 68: 6208-14. PMID 12895052 DOI: 10.1021/jo030075w  1
2003 Ellis TK, Hochla VM, Soloshonok VA. Efficient synthesis of 2-aminoindane-2-carboxylic acid via dialkylation of nucleophilic glycine equivalent. The Journal of Organic Chemistry. 68: 4973-6. PMID 12790614 DOI: 10.1021/jo030065v  1
2002 Hruby VJ, Qui W, Okayama T, Soloshonok VA. Design of nonpeptides from peptide ligands for peptide receptors. Methods in Enzymology. 343: 91-123. PMID 11665597 DOI: 10.1016/S0076-6879(02)43129-1  1
1997 Soloshonok VA, Ono T. Highly Enantioselective Transfer of Chirality from a Less to a More Configurationally Unstable Stereogenic Center. A Practical Asymmetric Synthesis of (Fluoroalkyl)amines via Biomimetic Transamination. The Journal of Organic Chemistry. 62: 3030-3031. PMID 11671677  0.36
1996 Ono T, Kukhar VP, Soloshonok VA. Biomimetic Reductive Amination of Fluoro Aldehydes and Ketones via [1,3]-Proton Shift Reaction.(1) Scope and Limitations. The Journal of Organic Chemistry. 61: 6563-6569. PMID 11667521  0.36
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