(Q41791232)

English

Stereoselective synthesis of alpha,alpha-chlorofluoro carbonyl compounds leading to the construction of fluorinated chiral quaternary carbon centers.

scientific article published on January 2008

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Stereoselective synthesis of alpha,alpha-chlorofluoro carbonyl compounds leading to the construction of fluorinated chiral quaternary carbon centers (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

stereoselectivity

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Kazutaka Shibatomi

1

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

author name string

Hisashi Yamamoto

2

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

language of work or name

0 references

publication date

1 January 2008

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Angewandte Chemie International Edition

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

47

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

31

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

5796-5798

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Catalytic asymmetric fluorination comes of age

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532067

6 June 2018

Fluorine in pharmaceuticals: looking beyond intuition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532067

6 June 2018

Enantioselective alpha-fluorination of carbonyl compounds: organocatalysis or metal catalysis?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532067

6 June 2018

Asymmetric fluorination, trifluoromethylation, and perfluoroalkylation reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532067

6 June 2018

Direct and enantioselective organocatalytic alpha-chlorination of aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532067

6 June 2018

Enantioselective organocatalytic alpha-fluorination of aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532067

18 August 2018

Highly enantioselective catalytic fluorination and chlorination reactions of carbonyl compounds capable of two-point binding.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532067

18 August 2018

Direct organocatalytic asymmetric alpha-chlorination of aldehydes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532067

18 August 2018

Asymmetric synthesis of chiral organofluorine compounds: use of nonracemic fluoroiodoacetic acid as a practical electrophile and its application to the synthesis of monofluoro hydroxyethylene dipeptide isosteres within a novel series of HIV protease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532067

18 August 2018

Improving Enantioselective Fluorination Reactions: Chiral N-Fluoroammonium Salts and Transition Metal Catalysts K.M. gratefully acknowledges generous support from Prof. Dr. K. H. Dötz and from the Fonds der Chemischen Industrie (Liebig stipend)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic enantioselective fluorination of beta-keto esters by phase-transfer catalysis using chiral quaternary ammonium salts

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An efficient enantioselective fluorination of various beta-ketoesters catalyzed by chiral palladium complexes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Titanium-catalyzed stereoselective geminal heterodihalogenation of beta-ketoesters

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly enantioselective direct organocatalytic alpha-chlorination of ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lewis acid-mediated selective chlorinations of silyl enolate

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective formation of stereogenic carbon-fluorine centers by a simple catalytic method

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct asymmetric alpha-fluorination of aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Construction of asymmetric fluorinated carbon centers

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic asymmetric fluorinations

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective Pd-catalyzed allylation reaction of fluorinated silyl enol ethers

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic Enantioselective Fluorination of β-Ketoesters

1 reference

https://pubmed.ncbi.nlm.nih.gov/18576459

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/ANIE.200801682

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18576459%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

ResearchGate publication ID

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