Enantioselective enzymatic desymmetrizations in organic synthesis
E García-Urdiales, I Alfonso, V Gotor - Chemical Reviews, 2005 - ACS Publications
During the recent past years, tremendous efforts have been made to establish
enantioselective routes for the preparation of enantiomerically pure compounds due to their …
enantioselective routes for the preparation of enantiomerically pure compounds due to their …
Role of conformational dynamics in the evolution of novel enzyme function
MA Maria-Solano, E Serrano-Hervás… - Chemical …, 2018 - pubs.rsc.org
The free energy landscape concept that describes enzymes as an ensemble of differently
populated conformational sub-states in dynamic equilibrium is key for evaluating enzyme …
populated conformational sub-states in dynamic equilibrium is key for evaluating enzyme …
A glimpse into green chemistry practices in the pharmaceutical industry
In this Minireview, the importance and implementation of green chemistry practices in the
pharmaceutical industry are illustrated. With notable examples, some of the most important …
pharmaceutical industry are illustrated. With notable examples, some of the most important …
Recent developments in asymmetric reduction of ketones with biocatalysts
K Nakamura, R Yamanaka, T Matsuda… - Tetrahedron: Asymmetry, 2003 - Elsevier
Herein we review recent advances in the asymmetric reduction of ketones by biocatalysts.
Included are discussions on recent developments in methodologies to control …
Included are discussions on recent developments in methodologies to control …
Eupergit® C, a carrier for immobilization of enzymes of industrial potential
E Katchalski-Katzir, DM Kraemer - Journal of molecular catalysis B …, 2000 - Elsevier
Eupergit® C is a carrier consisting of macroporous beads for immobilizing enzymes of
industrial potential for the production of fine chemicals and pharmaceuticals. Various …
industrial potential for the production of fine chemicals and pharmaceuticals. Various …
Enantioselective hydrogenation of dialkyl ketones
FH Zhang, FJ Zhang, ML Li, JH Xie, QL Zhou - Nature Catalysis, 2020 - nature.com
Chiral catalyst development is a key to asymmetric catalysis research. The enantioselectivity
of a chiral catalyst relies on its ability to distinguish the prochiral centres or faces of …
of a chiral catalyst relies on its ability to distinguish the prochiral centres or faces of …
Alcohol dehydrogenases as catalysts in organic synthesis
Alcohol dehydrogenases (ADHs) have become important catalysts for stereoselective
oxidation and reduction reactions of alcohols, aldehydes and ketones. The aim of this …
oxidation and reduction reactions of alcohols, aldehydes and ketones. The aim of this …
Regeneration of nicotinamide coenzymes: principles and applications for the synthesis of chiral compounds
A Weckbecker, H Gröger, W Hummel - Biosystems engineering I: creating …, 2010 - Springer
Dehydrogenases which depend on nicotinamide coenzymes are of increasing interest for
the preparation of chiral compounds, either by reduction of a prochiral precursor or by …
the preparation of chiral compounds, either by reduction of a prochiral precursor or by …
Modeling enzymatic enantioselectivity using quantum chemical methodology
The computational study of enantioselective reactions is a challenging task that requires
high accuracy, as very small energy differences have to be reproduced. Quantum chemical …
high accuracy, as very small energy differences have to be reproduced. Quantum chemical …
Chiral synthesis via organoboranes. 14. Selective reductions. 41. Diisopinocampheylchloroborane, an exceptionally efficient chiral reducing agent
HC Brown, J Chandrasekharan… - Journal of the …, 1988 - ACS Publications
Diisopinocampheylchloroborane, readily prepared in both enantiomers in high chemical
and optical purities (99% ee) via hydroboration followed by treatment with dry hydrogen …
and optical purities (99% ee) via hydroboration followed by treatment with dry hydrogen …