Enzyme Catalyzed Trans-Benzoin Condensation
Author(s) -
Gökçil BİLİR,
Ayhan S. Demir,
Salih Özçubukçu
Publication year - 2018
Publication title -
journal of the turkish chemical society section a chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.179
H-Index - 6
ISSN - 2149-0120
DOI - 10.18596/jotcsa.414603
Subject(s) - benzoin , chemistry , pseudomonas fluorescens , benzaldehyde , cofactor , catalysis , enzyme , organic chemistry , enantiomer , medicinal chemistry , stereochemistry , genetics , bacteria , biology
Benzaldehyde lyase (BAL) is an enzyme that is used in the C-C bond cleavage and formation which was isolated first from Pseudomonas fluorescens Biovar I. It requires thiamine diphosphate (ThDP) and Mg(II) ions as cofactors. In this work, BAL was used as an enzymatic catalysis for the trans-benzoin condensation reaction between racemic benzoins and benzyloxyacetaldehyde to form unsymmetrical benzoin products with moderate enantiomeric excesses. ( S )-benzoin derivatives remained unreacted at the end of the reaction. In this enzymatic trans-benzoin condensation, benzyloxyacetaldeyhde acted as acceptor and different variety of racemic benzoin derivatives were used as donor and ( R )-2-hydroxy-1-phenylpropanone derivatives were synthesized up to 66% ee.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom