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Organic Letters|April 10, 2009
New sterically driven mode for generation of helical chiralityHisanori Ueki, Vadim A SoloshonokJournal of the American Chemical Society|May 9, 2009
Resolution/deracemization of chiral alpha-amino acids using resolving reagents with flexible stereogenic centersVadim A Soloshonok, Trevor K Ellis, Hisanori Ueki, et al.Beilstein Journal of Organic Chemistry|December 5, 2012
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 bondsVadim A Soloshonok, José Luis Aceña, Hisanori Ueki, et al.The Journal of Organic Chemistry|July 17, 2004
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 prolinesVadim A Soloshonok, Hisanori Ueki, Rohit Tiwari, et al.The Journal of Organic Chemistry|October 27, 2006
Design, synthesis, and evaluation of a new generation of modular nucleophilic glycine equivalents for the efficient synthesis of sterically constrained alpha-amino acidsTrevor K Ellis, Hisanori Ueki, Takeshi Yamada, et al.Organic Letters|November 17, 2006
Efficient asymmetric synthesis of novel 4-substituted and configurationally stable analogues of thalidomideTakeshi Yamada, Takuya Okada, Kazuhiko Sakaguchi, et al.The Journal of Organic Chemistry|August 5, 2003
Efficient synthesis of serically constrained smmetrically alpha,alpha-disubstituted alpha-amino acids under operationally convenient conditionsTrevor K Ellis, Collin H Martin, Gary M Tsai, et al.Journal of the American Chemical Society|October 27, 2005
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 stereoselectivityVadim A Soloshonok, Chaozhong Cai, Takeshi Yamada, et al.The Journal of Organic Chemistry|August 30, 2003
Improved synthesis of proline-derived Ni(II) complexes of glycine: versatile chiral equivalents of nucleophilic glycine for general asymmetric synthesis of alpha-amino acidsHisanori Ueki, Trevor K Ellis, Collin H Martin, et al.Organic & Biomolecular Chemistry|May 30, 2013
Chemical approach for interconversion of (S)- and (R)-α-amino acidsAlexander E Sorochinsky, Hisanori Ueki, José Luis Aceña, et al.Pageof 15