(Q37305419)

19 August 2017

1 reference

title

Trifluoromethyl ethers--synthesis and properties of an unusual substituent (English)

1 reference

19 August 2017

Frédéric R Leroux

1

1 reference

19 August 2017

Baptiste Manteau

series ordinal

2

1 reference

19 August 2017

Jean-Pierre Vors

series ordinal

3

1 reference

19 August 2017

Sergiy Pazenok

series ordinal

4

1 reference

19 August 2017

29 April 2008

1 reference

Beilstein Journal of Organic Chemistry

19 August 2017

1 reference

19 August 2017

4

1 reference

19 August 2017

13

1 reference

Creative Commons Attribution 2.0 Generic

19 August 2017

start time

29 April 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

alpha-fluorinated ethers as "exotic" entity in medicinal chemistry.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

Mild electrophilic trifluoromethylation of carbon- and sulfur-centered nucleophiles by a hypervalent iodine(III)-CF3 reagent.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

Novel 10-I-3 hypervalent iodine-based compounds for electrophilic trifluoromethylation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

Alpha-fluorinated ethers, thioethers, and amines: anomerically biased species.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

Modern synthetic methods for fluorine-substituted target molecules

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

The 2 x 3 toolbox of organometallic methods for regiochemically exhaustive functionalization

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

Fluorine in medicinal chemistry

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

The unique role of fluorine in the design of active ingredients for modern crop protection

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

Electrophilic Perfluoroalkylating Agents

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

Molecular and cellular mechanisms of general anaesthesia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

Calculation of hydrophobic constant (log P) from .pi. and f constants

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

Trifluoromethoxy substituted anilines: metalation as the key step for structural elaboration.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

The trifluoromethoxy group: a long-range electron-withdrawing substituent

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

2-trifluoromethoxyethyl triflate: a versatile trifluoromethoxyethyl carrier

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2486484

Selective Fluorinations by Reagents Containing the OF Group

2 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18941485

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

CF3 oxonium salts, O-(trifluoromethyl)dibenzofuranium salts: in situ synthesis, properties, and application as a real CF3+ species reagent

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18941485

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3762/BJOC.4.13

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

18941485

1 reference