Highly Diastereo- and Enantioselective Synthesis of Trifluoromethyl-Substituted Cyclopropanes via Myoglobin-Catalyzed Transfer of Trifluoromethylcarbene. (Q48338923)

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scientific article published on 2 April 2017

Language	Label	Description	Also known as
English	Highly Diastereo- and Enantioselective Synthesis of Trifluoromethyl-Substituted Cyclopropanes via Myoglobin-Catalyzed Transfer of Trifluoromethylcarbene.	scientific article published on 2 April 2017

Statements

scholarly article

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

Highly Diastereo- and Enantioselective Synthesis of Trifluoromethyl-Substituted Cyclopropanes via Myoglobin-Catalyzed Transfer of Trifluoromethylcarbene. (English)

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

enantioselectivity

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

10 February 2018

http://europepmc.org/abstract/MED/28366001

4

1 reference

Europe PubMed Central

10 February 2018

http://europepmc.org/abstract/MED/28366001

author name string

Viktoria Steck

2

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

Vikas Tyagi

3

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

language of work or name

0 references

publication date

10 April 2017

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

Journal of the American Chemical Society

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

139

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

15

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

5293-5296

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

Recent Progress Toward the Synthesis of Trifluoromethyl- and Difluoromethyl-Substituted Cyclopropanes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

DNA-Accelerated Catalysis of Carbene-Transfer Reactions by a DNA/Cationic Iron Porphyrin Hybrid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

Biocatalytic Synthesis of Allylic and Allenyl Sulfides through a Myoglobin-Catalyzed Doyle-Kirmse Reaction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

Myoglobin-Catalyzed Olefination of Aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

Engineering a dirhodium artificial metalloenzyme for selective olefin cyclopropanation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

Intermolecular carbene S-H insertion catalysed by engineered myoglobin-based catalysts†.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

Highly diastereoselective and enantioselective olefin cyclopropanation using engineered myoglobin-based catalysts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

Myoglobin-catalyzed intermolecular carbene N-H insertion with arylamine substrates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

P450-catalyzed asymmetric cyclopropanation of electron-deficient olefins under aerobic conditions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

Improved cyclopropanation activity of histidine-ligated cytochrome P450 enables the enantioselective formal synthesis of levomilnacipran

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

Olefin Cyclopropanation via Carbene Transfer Catalyzed by Engineered Cytochrome P450 Enzymes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

Iron-catalyzed cyclopropanation with trifluoroethylamine hydrochloride and olefins in aqueous media: in situ generation of trifluoromethyl diazomethane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

16 June 2018

Gram-Scale Synthesis of Chiral Cyclopropane-Containing Drugs and Drug Precursors with Engineered Myoglobin Catalysts Featuring Complementary Stereoselectivity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

14 August 2018

An artificial metalloenzyme with the kinetics of native enzymes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

14 August 2018

Abiological catalysis by artificial haem proteins containing noble metals in place of iron

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

14 August 2018

Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

14 August 2018

Rhodium-catalyzed cyclopropenation of alkynes: synthesis of trifluoromethyl-substituted cyclopropenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

14 August 2018

Synthesis of trifluoromethyl-substituted proline analogues as 19F NMR labels for peptides in the polyproline II conformation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

14 August 2018

Diastereoselectivity controlled by electrostatic repulsion between the negative charge on a trifluoromethyl group and that on aromatic rings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5755966

14 August 2018

Synthesis of trifluoromethyl-substituted cyclopropanes via sequential Kharasch-dehalogenation reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/28366001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transition metal-catalyzed cyclopropanation of alkenes in water: catalyst efficiency and in situ generation of the diazo reagent

1 reference

https://pubmed.ncbi.nlm.nih.gov/28366001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

5,10,15,20-Tetraphenylporphyrinatorhodium(III) iodide catalyzed cyclopropanation reactions of alkenes using glycine ester hydrochloride

1 reference

https://pubmed.ncbi.nlm.nih.gov/28366001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copper-Catalyzed Insertion into Heteroatom-Hydrogen Bonds with Trifluorodiazoalkanes

1 reference

https://pubmed.ncbi.nlm.nih.gov/28366001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of Trifluoroethyl-Substituted Ketones from Aldehydes and Cyclohexanones

1 reference

https://pubmed.ncbi.nlm.nih.gov/28366001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective Cobalt-Catalyzed Preparation of Trifluoromethyl-Substituted Cyclopropanes

1 reference

https://pubmed.ncbi.nlm.nih.gov/28366001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of trans-2-(trifluoromethyl)cyclopropanes via Suzuki reactions with an N-methyliminodiacetic acid boronate

1 reference

https://pubmed.ncbi.nlm.nih.gov/28366001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JACS.7B00768

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

1 reference

Europe PubMed Central

15 June 2018

http://europepmc.org/abstract/PMC/5755966

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