Enzyme-mediated oxidations for the chemist
Biocatalysis is an enabling technology adding to organic oxidation chemistry. Especially the
high selectivity of enzymatic oxidation coevally operating under mild conditions and not …
high selectivity of enzymatic oxidation coevally operating under mild conditions and not …
Recent progress in biocatalysis for asymmetric oxidation and reduction
T Matsuda, R Yamanaka, K Nakamura - Tetrahedron: Asymmetry, 2009 - Elsevier
Recent progress in biocatalysis for asymmetric oxidation and reduction - ScienceDirect Skip to
main contentSkip to article Elsevier logo Journals & Books Search RegisterSign in View PDF …
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From a racemate to a single enantiomer: deracemization by stereoinversion
CC Gruber, I Lavandera, K Faber… - Advanced Synthesis & …, 2006 - Wiley Online Library
The stereoinversion of one enantiomer into its mirror‐image counterpart within a racemate
furnishes a single stereoisomeric product in 100% theoretical yield. This extremely efficient …
furnishes a single stereoisomeric product in 100% theoretical yield. This extremely efficient …
Biocatalysis
G Torrelo, U Hanefeld, F Hollmann - Catalysis Letters, 2015 - Springer
Biocatalysis is an enabling technology for chemists. Using isolated enzymes or whole cells
gives access to a broad range of selective transformations—often inaccessible with …
gives access to a broad range of selective transformations—often inaccessible with …
Candida parapsilosis: A versatile biocatalyst for organic oxidation-reduction reactions
This review highlights the importance of the biocatalyst, Candida parapsilosis for oxidation
and reduction reactions of organic compounds and establishes its versatility to generate a …
and reduction reactions of organic compounds and establishes its versatility to generate a …
Asymmetric reduction of aryl imines using Candida parapsilosis ATCC 7330
T Vaijayanthi, A Chadha - Tetrahedron: Asymmetry, 2008 - Elsevier
A highly enantioselective one pot, novel biocatalytic method for the asymmetric reduction of
aryl imines is reported. Treatment of aryl imines with Candida parapsilosis ATCC 7330 in …
aryl imines is reported. Treatment of aryl imines with Candida parapsilosis ATCC 7330 in …
Unexpected stereorecognition in nitrilase-catalyzed hydrolysis of β-hydroxy nitriles
S Kamila, D Zhu, ER Biehl, L Hua - Organic Letters, 2006 - ACS Publications
Biocatalytic enantioselective hydrolysis of β-hydroxy nitriles to corresponding (S)-enriched β-
hydroxy carboxylic acids has been achieved for the first time by an isolated nitrilase bll6402 …
hydroxy carboxylic acids has been achieved for the first time by an isolated nitrilase bll6402 …
Asymmetric reduction of alkyl 2-oxo-4-arylbutanoates and-but-3-enoates by Candida parapsilosis ATCC 7330: assignment of the absolute configuration of ethyl 2 …
Enantioselective bioreduction of alkyl 2-oxo-4-arylbutanoates and 2-oxo-4-arylbut-3-
enoates mediated by Candida parapsilosis ATCC 7330 resulted in the formation of the …
enoates mediated by Candida parapsilosis ATCC 7330 resulted in the formation of the …
Enantiomerically pure allylic alcohols: preparation by Candida parapsilosis ATCC 7330 mediated deracemisation
Enantiomerically pure allylic alcohols: preparation by Candida parapsilosis ATCC 7330
mediated deracemisation - ScienceDirect Skip to main contentSkip to article Elsevier logo …
mediated deracemisation - ScienceDirect Skip to main contentSkip to article Elsevier logo …
One-pot synthesis of enantiomerically pure 1, 2-diols: asymmetric reduction of aromatic α-oxoaldehydes catalysed by Candida parapsilosis ATCC 7330
P Mahajabeen, A Chadha - Tetrahedron: Asymmetry, 2011 - Elsevier
A facile and simple one-pot method was developed to produce a series of optically active (S)-
1-phenyl-1, 2-ethanediols with good yields (up to 70%) and high enantiomeric excess (> …
1-phenyl-1, 2-ethanediols with good yields (up to 70%) and high enantiomeric excess (> …