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Quantitative Structure−Activity Relationships for the Enantioselectivity of Oxirane Ring-Opening Catalyzed by Epoxide Hydrolases

https://doi.org/10.1021/ci020047z

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What this work says

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Microbiological transformations-XXIX. Enantioselective hydrolysis of epoxides using microorganisms: A mechanistic study

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3-D QSAR analysis of inhibition of murine soluble epoxide hydrolase (MsEH) by benzoylureas, arylureas, and their analogues

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Molecular modeling and biocatalysis: explanations, predictions, limitations, and opportunities

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Fungal epoxide hydrolases: new tools for the synthesis of enantiopure epoxides and diols

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Bacterial epoxide hydrolases of opposite enantiopreference

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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Bibliography

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Quantitative Structure—Activity Realtionships for the Enantioselectivity of Oxirane Ring‐Opening Catalyzed by Epoxide Hydrolases.

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Data mining and enantiophore studies on chiral stationary phases used in HPLC separation

inferred← citeshttps://doi.org/10.1002/chir.20281openalex-snapshot

Enantiophore modeling in 3D‐QSAR. A data mining application on Whelk‐O1 chiral stationary phase

inferred← citeshttps://doi.org/10.1002/jssc.200800693openalex-snapshot

Exploring enantioselective molecular recognition mechanisms with chemoinformatic techniques

inferred← citeshttps://doi.org/10.1002/qsar.200810066openalex-snapshot

Encoding Absolute Configurations with Chiral Enantiophore Descriptors. Application to the Order of Elution of Enantiomers in Liquid Chromatography

inferred← citeshttps://doi.org/10.1007/s10822-006-9042-6openalex-snapshot

Application of artificial neural networks and DFT-based parameters for prediction of reaction kinetics of ethylbenzene dehydrogenase

inferred← citeshttps://doi.org/10.1007/s10822-017-0090-xopenalex-snapshot

Learning epistatic interactions from sequence-activity data to predict enantioselectivity

inferred← citeshttps://doi.org/10.1007/s11030-008-9068-xopenalex-snapshot

Counter propagation artificial neural networks modeling of an enantioselectivity of artificial metalloenzymes

inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00103-6openalex-snapshot

Oxiranes and Oxirenes: Monocyclic

inferred← citeshttps://doi.org/10.1016/j.bmc.2013.04.044openalex-snapshot

Predicting CYP2C19 catalytic parameters for enantioselective oxidations using artificial neural networks and a chirality code

inferred← citeshttps://doi.org/10.1016/j.chroma.2008.01.034openalex-snapshot

Simple method for the prediction of the separation of racemates with high-performance liquid chromatography on Whelk-O1 chiral stationary phase

inferred← citeshttps://doi.org/10.1016/j.micromeso.2011.06.011openalex-snapshot

A quantitative structure activity relationship approach to probe the influence of the functionalization on the drug encapsulation of porous metal-organic frameworks

inferred← citeshttps://doi.org/10.1016/j.tetasy.2003.12.013openalex-snapshot

Oxazaborolidine mediated asymmetric ketone reduction: prediction of enantiomeric excess based on catalyst structure

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Prediction of enzyme activity with neural network models based on electronic and geometrical features of substrates

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Exploring Phase-Transfer Catalysis with Molecular Dynamics and 3D/4D Quantitative Structure−Selectivity Relationships

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Rationalization of the entrapping of bioactive molecules into a series of functionalized porous zirconium terephthalate MOFs

inferred← citeshttps://doi.org/10.1039/c5em00084jopenalex-snapshot

Quantitative structure–activity relationship correlation between molecular structure and the Rayleigh enantiomeric enrichment factor

inferred← citeshttps://doi.org/10.1109/bigdata.2013.6691756openalex-snapshot

KUChemBio: A repository of computational chemical biology data sets

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