(Q41144486)

27 September 2017

Nitrile as Activating Group in the Asymmetric Bioreduction of β-Cyanoacrylic Acids Catalyzed by Ene-Reductases (English)

1 reference

27 September 2017

5

1 reference

27 September 2017

Horst Lechner

4

0 references

Christoph Winkler

object named as

Christoph K Winkler

1

0 references

author name string

Dorina Clay

2

1 reference

27 September 2017

Nikolaus G Turrini

3

1 reference

27 September 2017

Simon Davies

6

1 reference

27 September 2017

Sebastien Debarge

7

1 reference

27 September 2017

Pat O'Neill

8

1 reference

27 September 2017

Jeremy Steflik

9

1 reference

27 September 2017

Mike Karmilowicz

10

1 reference

27 September 2017

John W Wong

11

1 reference

27 September 2017

Kurt Faber

12

1 reference

27 September 2017

language of work or name

1 reference

9 April 2014

1 reference

Advanced Synthesis & Catalysis

27 September 2017

1 reference

27 September 2017

356

1 reference

27 September 2017

8

1 reference

27 September 2017

1878-1882

1 reference

Chemoenzymatic asymmetric synthesis of pregabalin precursors via asymmetric bioreduction of β-cyanoacrylate esters using ene-reductases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

Asymmetric bioreduction of activated alkenes to industrially relevant optically active compounds.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

Asymmetric Reduction of Activated Alkenes by Pentaerythritol Tetranitrate Reductase: Specificity and Control of Stereochemical Outcome by Reaction Optimisation.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

Crystal structure of a thermostable old yellow enzyme from Thermus scotoductus SA-01

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

Site-saturation mutagenesis of tryptophan 116 of Saccharomyces pastorianus old yellow enzyme uncovers stereocomplementary variants

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

A novel chromate reductase from Thermus scotoductus SA-01 related to old yellow enzyme.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

Asymmetric bioreduction of activated C=C bonds using enoate reductases from the old yellow enzyme family.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

Crystal structure of 12-oxophytodienoate reductase 3 from tomato: self-inhibition by dimerization

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

On the active site of Old Yellow Enzyme. Role of histidine 191 and asparagine 194

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

Asymmetric bioreduction of alkenes using ene-reductases YersER and KYE1 and effects of organic solvents

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

The 1.3 A crystal structure of the flavoprotein YqjM reveals a novel class of Old Yellow Enzymes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

Asymmetric catalysis: science and opportunities (Nobel lecture).

14 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

Asymmetric alkene reduction by yeast old yellow enzymes and by a novel Zymomonas mobilis reductase.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4498475

Stereocomplementary Bioreduction of α,β-Unsaturated Dicarboxylic Acids and Dimethyl Esters using Enoate Reductases: Enzyme- and Substrate-Based Stereocontrol

19 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FADSC.201301055

Asymmetric Bioreduction of Activated Alkenes Using Cloned 12-Oxophytodienoate Reductase Isoenzymes OPR-1 and OPR-3 fromLycopersicon esculentum (Tomato): A Striking Change of Stereoselectivity

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FADSC.201301055

The flavoprotein-catalyzed reduction of aliphatic nitro-compounds represents a biocatalytic equivalent to the Nef-reaction

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FADSC.201301055

Chemistry. The organic approach to asymmetric catalysis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26190962

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The oxidative half-reaction of Old Yellow Enzyme. The role of tyrosine 196

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26190962

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A substrate-driven approach to determine reactivities of α,β-unsaturated carboxylic esters towards asymmetric bioreduction

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26190962

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/ADSC.201301055

1 reference

27 September 2017

1 reference

27 September 2017

1 reference