| Year |
Citation |
Score |
| 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 |
0.6 |
|
| 2014 |
Maestro MA, Avecilla F, Sorochinsky AE, Ellis TK, Aceña JL, Soloshonok VA. 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. DOI: 10.1002/Ejoc.201402145 |
0.447 |
|
| 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 |
0.605 |
|
| 2013 |
Sorochinsky AE, Ueki H, Aceña JL, Ellis TK, Moriwaki H, Sato T, Soloshonok VA. Chemical deracemization and (S) to (R) interconversion of some fluorine-containing α-amino acids Journal of Fluorine Chemistry. 152: 114-118. DOI: 10.1016/J.Jfluchem.2013.02.022 |
0.62 |
|
| 2010 |
Soloshonok VA, Ueki H, Ellis TK. 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. DOI: 10.1002/chin.201001243 |
0.626 |
|
| 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 |
0.606 |
|
| 2009 |
Soloshonok VA, Ueki H, Ellis TK. New generation of modular nucleophilic glycine equivalents for the general synthesis of α-amino acids Synlett. 0704-0715. DOI: 10.1055/S-0028-1087929 |
0.686 |
|
| 2009 |
Soloshonok VA, Ueki H, Ellis TK. 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. DOI: 10.1021/bk-2009-1009.ch005 |
0.503 |
|
| 2009 |
Ellis TK, Ueki H, Tiwari R, Soloshonok VA. 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. DOI: 10.1016/J.Tetasy.2009.10.006 |
0.64 |
|
| 2009 |
Soloshonok VA, Ueki H, Ellis TK. ChemInform Abstract: Modular Approach to the Design of Nucleophilic Glycine Equivalents with Tailorable Physicochemical Properties Cheminform. 40: no-no. DOI: 10.1002/chin.200951242 |
0.441 |
|
| 2009 |
Soloshonok VA, Ueki H, Ellis TK. ChemInform Abstract: New Generation of Modular Nucleophilic Glycine Equivalents for the General Synthesis of α-Amino Acids Cheminform. 40. DOI: 10.1002/chin.200927249 |
0.62 |
|
| 2008 |
Soloshonok VA, Ueki H, Ellis TK. Modular approach to the design of nucleophilic glycine equivalents with tailorable physico-chemical properties Chimica Oggi. 26: 51-54. |
0.354 |
|
| 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 |
0.521 |
|
| 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 |
0.64 |
|
| 2006 |
Ellis TK, Soloshonok VA. Design and synthesis of a new generation of 'NH'-Ni(II) complexes of glycine Schiff bases and their unprecedented C-H vs. N-H chemoselectivity in alkyl halide alkylations and Michael addition reactions Synlett. 533-538. DOI: 10.1055/S-2006-926252 |
0.626 |
|
| 2005 |
Soloshonok VA, Ueki H, Ellis TK, Yamada T, Ohfune Y. Application of modular nucleophilic glycine equivalents for truly practical asymmetric synthesis of β-substituted pyroglutamic acids Tetrahedron Letters. 46: 1107-1110. DOI: 10.1016/J.Tetlet.2004.12.093 |
0.671 |
|
| 2005 |
Ellis TK, Ueki H, Soloshonok VA. New generation of nucleophilic glycine equivalents Tetrahedron Letters. 46: 941-944. DOI: 10.1016/J.Tetlet.2004.12.050 |
0.558 |
|
| 2005 |
Soloshonok VA, Ueki H, Ellis TK, Yamada T, Ohfune Y. Application of Modular Nucleophilic Glycine Equivalents for Truly Practical Asymmetric Synthesis of β-Substituted Pyroglutamic Acids. Cheminform. 36. DOI: 10.1002/chin.200523200 |
0.601 |
|
| 2005 |
Berbasov DO, Ellis TK, Soloshonok VA. Biocatalytic Entry to Enantiomerically Pure β-Amino Acids Enantioselective Synthesis of β-Amino Acids: Second Edition. 397-414. DOI: 10.1002/0471698482.ch17 |
0.56 |
|
| 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 |
0.614 |
|
| 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 |
0.525 |
|
| 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 |
0.651 |
|
| 2003 |
Ellis TK, Martin CH, Ueki H, Soloshonok VA. Efficient, practical synthesis of symmetrically α,α-disubstituted α-amino acids Tetrahedron Letters. 44: 1063-1066. DOI: 10.1016/S0040-4039(02)02719-3 |
0.626 |
|
| 2003 |
Ueki H, Ellis TK, Khan MA, Soloshonok VA. Highly diastereoselective synthesis of new, carbostyril-based type of conformationally-constrained β-phenylserines Tetrahedron. 59: 7301-7306. DOI: 10.1016/S0040-4020(03)01172-4 |
0.593 |
|
| 2003 |
Ueki H, Ellis TK, Martin CH, Soloshonok VA. Efficient large-scale synthesis of picolinic acid-derived nickel(II) complexes of glycine European Journal of Organic Chemistry. 1954-1957. DOI: 10.1002/Ejoc.200200688 |
0.533 |
|
| 2003 |
Ueki H, Ellis T, Martin C, Soloshonok V. Efficient Large-Scale Synthesis of Picolinic Acid-Derived Nickel(II) Complexes of Glycine European Journal of Organic Chemistry. 2003: 1954-1957. DOI: 10.1002/ejoc.200200688 |
0.55 |
|
| 2003 |
Ellis TK, Martin CH, Tsai GM, Ueki H, Soloshonok VA. Efficient Synthesis of Sterically Constrained Symmetrically α,α-Disubstituted α-Amino Acids under Operationally Convenient Conditions. Cheminform. 34. DOI: 10.1002/chin.200349071 |
0.556 |
|
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