Substituent effects on the stereochemical outcome of the baker's yeast-mediated biotransformation of α-hydroxy- and α-acetoxymethyl-5-phenylfuran-2-yl-ethanones

Tetrahedron Asymmetry

Volumn 21, Issue 3, 2010, Pages 356-364

  Bencze, László Csaba ^a   Paizs, Csaba ^a   Toşa, Monica Ioana ^a   Irimie, Florin Dan ^a  

^a BABE BOLYAI UNIVERSITY   (Romania)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA ACETOXYMETHYL 5 PHENYLFURAN 2 YL ETHANONE DERIVATIVE; ALPHA HYDROXY 5 PHENYLFURAN 2 YL ETHANONE DERIVATIVE; FURAN DERIVATIVE; KETONE DERIVATIVE; PHENYL GROUP; UNCLASSIFIED DRUG;

ARTICLE; BIOTRANSFORMATION; CARBON NUCLEAR MAGNETIC RESONANCE; CELL TRANSFORMATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; REDUCTION; SACCHAROMYCES CEREVISIAE; STEREOCHEMISTRY; SYNTHESIS;

EID: 77949292835     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2010.02.004     Document Type: Article

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