The enantioselective hydrogenation of ethyl pyruvate using a Pt/SiO2 catalyst modified with six different chiral modifiers was studied. The chiral modifiers chosen were: (S)-(+)-1-aminoindan, (R)-(-)-1-aminoindan, (1 R,2S)-(+)-cis-1- amino-2-indanol, (1S,2R)-(-)-cis-1-amino-2-indanol, (S)-(+)-1-indanol and (R)-(-)-1-indanol.An excess of the (R) enantiomer of the product of 63% and 45% with (S)-(+)-1-aminoindan and (R)-(-)-1-aminoindan modifiers, respectively was obtained. When using (15,2R)-(-)-cis-1-amino-2-indanol and (1R,25)-(+)-cis-1-amino-2-indanol, the enantiomeric excess (ee%) obtained was 30% and 5%, respectively, while with both indanols ee% did not exceed 8%. Molecular modeling of the complex formed between the chiral modifier and ethyl pyruvate performed by DFT calculations allowed predicting the values of ee% obtained experimentally. The low ee% value obtained both aminoindanol chiral modifiers were used, could be explained by the analysis of non-covalent interactions (NCI) method. These calculations demonstrated the presence of an intramolecular hydrogen bond in the structure of these modifiers. (C) 2016 Elsevier B.V. All rights reserved.