Cross-Coupling of Mesylated Phenol Derivatives with Potassium Cyclopropyltrifluoroborate (Q35250631)

From Wikidata

Jump to navigation Jump to search

scientific article published on September 2, 2011

edit

Language	Label	Description	Also known as
English	Cross-Coupling of Mesylated Phenol Derivatives with Potassium Cyclopropyltrifluoroborate	scientific article published on September 2, 2011

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

title

Cross-coupling of mesylated phenol derivatives with potassium cyclopropyltrifluoroborate (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

Cross-Coupling of Mesylated Phenol Derivatives with Potassium Cyclopropyltrifluoroborate (English)

1 reference

stated in

Crossref

DOI

10.1021/JO2015246

reference URL

https://api.crossref.org/works/10.1021/JO2015246

retrieved

11 December 2024

author

Gary A. Molander

series ordinal

1

object named as

Gary A Molander

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

Terren K Niethamer

series ordinal

3

object named as

Terren K. Niethamer

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21888362

retrieved

11 December 2024

author name string

Floriane Beaumard

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

language of work or name

English

0 references

publication date

2 September 2011

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

full work available at URL

https://europepmc.org/articles/pmc3184376?pdf=render

file format

Portable Document Format

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21888362

retrieved

11 December 2024

https://europepmc.org/articles/PMC3184376

file format

HyperText Markup Language

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21888362

retrieved

11 December 2024

https://europepmc.org/articles/PMC3184376?pdf=render

file format

Portable Document Format

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21888362

retrieved

11 December 2024

https://doi.org/10.1021/jo2015246

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21888362

retrieved

11 December 2024

https://pubs.acs.org/doi/pdf/10.1021/jo2015246

1 reference

stated in

Crossref

DOI

10.1021/JO2015246

reference URL

https://api.crossref.org/works/10.1021/JO2015246

retrieved

11 December 2024

published in

Journal of Organic Chemistry

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

volume

76

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

issue

19

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

page(s)

8126-8130

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

cites work

Cross-coupling of mesylated phenol derivatives with potassium alkoxymethyltrifluoroborates

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Cross-Coupling of Mesylated Phenol Derivatives with Potassium Ammonio- and Amidomethyltrifluoroborates

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Nickel-catalyzed cross-couplings involving carbon-oxygen bonds

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Nickel-catalyzed C-O activation of phenol derivatives with potassium heteroaryltrifluoroborates

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Aryl trifluoroborates in Suzuki-Miyaura coupling: the roles of endogenous aryl boronic acid and fluoride

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

A versatile catalyst system for Suzuki-Miyaura cross-coupling reactions of C(sp(2))-tosylates and mesylates

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Cross-coupling of cyclopropyl- and cyclobutyltrifluoroborates with aryl and heteroaryl chlorides

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Biaryl Phosphane Ligands in Palladium-Catalyzed Amination

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Potassium organotrifluoroborates: new perspectives in organic synthesis.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Regioselective (site-selective) functionalization of unsaturated halogenated nitrogen, oxygen and sulfur heterocycles by Pd-catalysed cross-couplings and direct arylation processes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Organotrifluoroborates: protected boronic acids that expand the versatility of the Suzuki coupling reaction

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

27 July 2018

Aminopyrazine Inhibitors Binding to an Unusual Inactive Conformation of the Mitotic Kinase Nek2: SAR and Structural Characterization

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

26 September 2018

A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

26 September 2018

GPR109a agonists. Part 1: 5-Alkyl and 5-aryl-pyrazole-tetrazoles as agonists of the human orphan G-protein coupled receptor GPR109a

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

26 September 2018

Biosynthesis and Metabolism of Cyclopropane Rings in Natural Compounds

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3184376

retrieved

26 September 2018

Palladium-catalyzed cross-coupling of stereospecific potassium cyclopropyl trifluoroborates with aryl bromides

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21888362

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transition metal chemistry of cyclopropenes and cyclopropanes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21888362

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A general palladium catalyst system for Suzuki-Miyaura coupling of potassium aryltrifluoroborates and aryl mesylates

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21888362

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ligand effects in bimetallic high oxidation state palladium systems

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21888362

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient Suzuki-Type Cross-Coupling of Enantiomerically Pure Cyclopropylboronic Acids

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21888362

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

series ordinal

6

1 reference

stated in

Crossref

DOI

10.1021/JO2015246

reference URL

https://api.crossref.org/works/10.1021/JO2015246

retrieved

11 December 2024

Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998

series ordinal

8

1 reference

stated in

Crossref

DOI

10.1021/JO2015246

reference URL

https://api.crossref.org/works/10.1021/JO2015246

retrieved

11 December 2024

Palladium-catalyzed cross-coupling of cyclopropylboronic acids with alkenyl triflates

series ordinal

25

1 reference

stated in

Crossref

DOI

10.1021/JO2015246

reference URL

https://api.crossref.org/works/10.1021/JO2015246

retrieved

11 December 2024

Identifiers

DOI

10.1021/JO2015246

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

PMC publication ID

3184376

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

PubMed publication ID

21888362

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21888362

retrieved

7 August 2017

ResearchGate publication ID

51615763

0 references

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q35250631&oldid=2285997943"