(Q41765733)

English

A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids

scientific article published on October 2010

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids (English)

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

object named as

boronic acids

15 July 2023

Stephen L. Buchwald

3

object named as

Stephen L Buchwald

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

author name string

Tom Kinzel

1

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Yong Zhang

2

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

language of work or name

0 references

publication date

1 October 2010

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Journal of the American Chemical Society

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

132

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

40

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

14073-14075

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

6 June 2018

Structure-activity relationships of monomeric C2-aryl pyrrolo[2,1-c][1,4]benzodiazepine (PBD) antitumor agents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

6 June 2018

Scope of the Suzuki-Miyaura cross-coupling reactions of potassium heteroaryltrifluoroborates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

6 June 2018

A new class of easily activated palladium precatalysts for facile C-N cross-coupling reactions and the low temperature oxidative addition of aryl chlorides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

6 June 2018

Copper-catalyzed arylation and alkenylation of polyfluoroarene C-H bonds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

6 June 2018

A convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chlorides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

6 June 2018

Catalysts for Suzuki-Miyaura coupling processes: scope and studies of the effect of ligand structure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

6 June 2018

Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of potassium aryl- and heteroaryltrifluoroborates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

6 June 2018

Pyrazole acids as niacin receptor agonists for the treatment of dyslipidemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

18 August 2018

Combined directed ortho and remote metalation-Suzuki cross-coupling strategies. Efficient synthesis of heteroaryl-fused benzopyranones from biaryl O-carbamates.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

18 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

18 August 2018

Cyclic triolborates: air- and water-stable ate complexes of organoboronic acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

18 August 2018

Aryl-substituted C3-bridged oligopyrroles as anion receptors for formation of supramolecular organogels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

18 August 2018

One-pot oxidation and bromination of 3,4-diaryl-2,5-dihydrothiophenes using Br2: synthesis and application of 3,4-diaryl-2,5-dibromothiophenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

18 August 2018

A highly active catalyst for Suzuki-Miyaura cross-coupling reactions of heteroaryl compounds.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

18 August 2018

Structure-activity relationships for 2-anilino-6-phenylpyrido[2,3-d]pyrimidin-7(8H)-ones as inhibitors of the cellular checkpoint kinase Wee1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2953245

18 August 2018

An efficient synthesis and substitution of 3-aroyl-2-bromobenzo[b]furans

1 reference

https://pubmed.ncbi.nlm.nih.gov/20858009

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pd-PEPPSI-IPent: an active, sterically demanding cross-coupling catalyst and its application in the synthesis of tetra-ortho-substituted biaryls

1 reference

https://pubmed.ncbi.nlm.nih.gov/20858009

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mild and general conditions for the cross-coupling of aryl halides with pentafluorobenzene and other perfluoroaromatics

1 reference

https://pubmed.ncbi.nlm.nih.gov/20858009

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly efficient monophosphine-based catalyst for the palladium-catalyzed suzuki-miyaura reaction of heteroaryl halides and heteroaryl boronic acids and esters

1 reference

https://pubmed.ncbi.nlm.nih.gov/20858009

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suzuki−Miyaura Coupling Reaction Using Pentafluorophenylboronic Acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/20858009

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA1073799

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q41765733&oldid=1934759844"