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Trevor K. Ellis, Ph.D.

Affiliations: 
2007 Department of Chemistry and Biochemistry University of Oklahoma, Norman, OK, United States 
Area:
Organic Chemistry
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"Trevor Ellis"
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Vadim A. Soloshonok grad student 2007 University of Oklahoma
 (Synthesis of symmetrical and optically active alpha-amino acids via homologation of nickel(II) complexed glycine Schiff bases.)

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Bergagnini M, Fukushi K, Han J, et al. (2014) NH-type of chiral Ni(II) complexes of glycine Schiff base: design, structural evaluation, reactivity and synthetic applications. Organic & Biomolecular Chemistry. 12: 1278-91
Maestro MA, Avecilla F, Sorochinsky AE, et al. (2014) Chiral N(H)-tBu and N(H)-Ad NiII complexes of glycine schiff bases: Deduction of a mode of kinetic diastereoselectivity European Journal of Organic Chemistry. 2014: 4309-4314
Sorochinsky AE, Ueki H, Aceña JL, et al. (2013) Chemical approach for interconversion of (S)- and (R)-α-amino acids. Organic & Biomolecular Chemistry. 11: 4503-7
Sorochinsky AE, Ueki H, Aceña JL, et al. (2013) Chemical deracemization and (S) to (R) interconversion of some fluorine-containing α-amino acids Journal of Fluorine Chemistry. 152: 114-118
Soloshonok VA, Ueki H, Ellis TK. (2010) ChemInform Abstract: Michael Addition Reactions Between Nucleophilic Glycine Equivalents and Acrylic Acid Derivatives as a Practical and Generalized Approach to the Asymmetric Synthesis of β-Substituted α-Amino Acids Cheminform. 41: no-no
Soloshonok VA, Ellis TK, Ueki H, et al. (2009) Resolution/deracemization of chiral alpha-amino acids using resolving reagents with flexible stereogenic centers. Journal of the American Chemical Society. 131: 7208-9
Soloshonok VA, Ueki H, Ellis TK. (2009) New generation of modular nucleophilic glycine equivalents for the general synthesis of α-amino acids Synlett. 0704-0715
Soloshonok VA, Ueki H, Ellis TK. (2009) Michael addition reactions between nucleophilic glycine equivalents and acrylic acid derivatives as a practical and generalized approach to the asymmetric synthesis of β-substituted-α-amino acids Acs Symposium Series. 1009: 72-88
Ellis TK, Ueki H, Tiwari R, et al. (2009) Michael addition reactions between various nucleophilic glycine equivalents and (S,E)-1-enoyl-5-oxo-N-phenylpyrrolidine-2-carboxamide, an optimal type of chiral Michael acceptor in the asymmetric synthesis of β-phenyl pyroglutamic acid and related compounds Tetrahedron Asymmetry. 20: 2629-2634
Soloshonok VA, Ueki H, Ellis TK. (2009) ChemInform Abstract: Modular Approach to the Design of Nucleophilic Glycine Equivalents with Tailorable Physicochemical Properties Cheminform. 40: no-no
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