Results 1 - 10 of 52

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• B. Samas, W. Wang and D. B. Godrej. 1:1 Cocrystal of (S)-3-(ammoniomethyl)-5-methylhexanoate and (S)-mandelic acid, Acta Cryst. (2007). E63, o3938    

  [DOI: 10.1107/S1600536807041803]
  
• M.-Y. Teng, J. Sun, C.-A. Ma and Q.-B. Song. (S)-2-Hydroxy-2-phenylacetic acid-(R)-2-aminobutanoic acid-water (1/1/0.5), Acta Cryst. (2006). E62, o2454-o2456    

  [DOI: 10.1107/S1600536806018605]
  
• Hong-Qing Hao, Wen-Ting Liu, Wei Tan, Zhuo-Jia Lin and Ming-Liang Tong. Spontaneous resolution of chiral metal mandelates by stereochemical control, CrystEngComm, 2009, 11, 967.

  [DOI: 10.1039/b822506k]
  
• Gonzalo Blay, Luz Cardona, Isabel Fernández, Alícia Marco-Aleixandre, M. Carmen Muñoz and José R. Pedro. Catalytic enantioselective addition of terminal alkynes to aromatic aldehydes using zinc-hydroxyamide complexes, Org. Biomol. Chem., 2009, 7, 4301.

  [DOI: 10.1039/b911592g]
  
• Gennaro Pescitelli, Lorenzo Di Bari and Nina Berova. Conformational aspects in the studies of organic compounds by electronic circular dichroism, Chem. Soc. Rev., 2011, 40, 4603.

  [DOI: 10.1039/c1cs15036g]
  
• Roger A. Sheldon. Green solvents for sustainable organic synthesis: state of the art, Green Chem., 2005, 7, 267.

  [DOI: 10.1039/b418069k]
  
• [DOI: 10.1016/S0960-894X(03)00311-1]
  
• Exploring the Potential of Fungal Arylacetonitrilases in Mandelic Acid Synthesis, Molecular Biotechnology

  [DOI: 10.1007/s12033-015-9840-y]
  
• Highly efficient conversion of (??)-mandelic acid to its (R)-(???)-enantiomer by combination of enzyme-mediated oxidation and reduction, Biotechnology Letters

  [DOI: 10.1007/BF01027017]
  
• Enantioselective oxidation of mandelic acid using a phenylmalonate metabolizing pathway of a soil bacteriumAlcaligenesnbronchisepticus KU 1201, Biotechnology Letters

  [DOI: 10.1007/BF01021248]