Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides (Q29302487)

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English	Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides	scientific article (publication date: 18 November 2008)

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title

Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides (English)

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DOI.org query endpoint

reference URL

https://doi.org/10.1021%2FAR800098P

retrieved

9 April 2017

author

John F. Hartwig

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John F. Hartwig

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DOI.org query endpoint

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9 April 2017

language of work or name

English

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publication date

18 November 2008

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reference URL

https://doi.org/10.1021%2FAR800098P

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9 April 2017

published in

Accounts of Chemical Research

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reference URL

https://doi.org/10.1021%2FAR800098P

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9 April 2017

volume

41

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DOI.org query endpoint

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https://doi.org/10.1021%2FAR800098P

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9 April 2017

issue

11

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https://doi.org/10.1021%2FAR800098P

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9 April 2017

page(s)

1534-1544

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https://doi.org/10.1021%2FAR800098P

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9 April 2017

cites work

Monodentate Phosphines Provide Highly Active Catalysts for Pd-Catalyzed CN Bond-Forming Reactions of Heteroaromatic Halides/Amines and (H)N-Heterocycles

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PubMed Central

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9 April 2017

Expanding Pd-catalyzed C-N bond-forming processes: the first amidation of aryl sulfonates, aqueous amination, and complementarity with Cu-catalyzed reactions

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PubMed Central

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9 April 2017

Palladium-Catalyzed α-Arylation of Carbonyl Compounds and Nitriles

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9 April 2017

Highly reactive, general and long-lived catalysts for palladium-catalyzed amination of heteroaryl and aryl chlorides, bromides, and iodides: scope and structure-activity relationships

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3 June 2018

Reductive elimination of ether from T-shaped, monomeric arylpalladium alkoxides

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3 June 2018

Electronic effects on reductive elimination to form carbon-carbon and carbon-heteroatom bonds from palladium(II) complexes

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PubMed Central

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3 June 2018

Highly reactive, general, and long-lived catalysts for coupling heteroaryl and aryl chlorides with primary nitrogen nucleophiles

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PubMed Central

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26 November 2018

Palladium-catalyzed arylation of trimethylsilyl enolates of esters and imides. High functional group tolerance and stereoselective synthesis of alpha-aryl carboxylic acid derivatives

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PubMed Central

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26 November 2018

Oxidative addition of aryl tosylates to palladium(0) and coupling of unactivated aryl tosylates at room temperature

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PubMed Central

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26 November 2018

Unparalleled Rates for the Activation of Aryl Chlorides and Bromides: Coupling with Amines and Boronic Acids in Minutes at Room Temperature

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PubMed Central

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26 November 2018

Air stable, sterically hindered ferrocenyl dialkylphosphines for palladium-catalyzed C[bond]C, C[bond]N, and C[bond]O bond-forming cross-couplings

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PubMed Central

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26 November 2018

Scope and limitations of the Pd/BINAP-catalyzed amination of aryl bromides

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18681463

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12 December 2020

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Simple, Efficient Catalyst System for the Palladium-Catalyzed Amination of Aryl Chlorides, Bromides, and Triflates

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

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12 December 2020

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The Synthesis of Aminopyridines: A Method Employing Palladium-Catalyzed Carbon-Nitrogen Bond Formation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

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12 December 2020

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Room-Temperature Palladium-Catalyzed Amination of Aryl Bromides and Chlorides and Extended Scope of Aromatic C−N Bond Formation with a Commercial Ligand

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved functional group compatibility in the palladium-catalyzed synthesis of aryl amines

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

P(i-BuNCH2CH2)3N: an effective ligand in the palladium-catalyzed amination of aryl bromides and iodides

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis, structure, and reductive elimination chemistry of three-coordinate arylpalladium amido complexes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A general and long-lived catalyst for the palladium-catalyzed coupling of aryl halides with thiols

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Modified (NHC)Pd(allyl)Cl (NHC =N-Heterocyclic Carbene) Complexes for Room-Temperature Suzuki−Miyaura and Buchwald−Hartwig Reactions

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palladium-catalyzed intermolecular alpha-arylation of zinc amide enolates under mild conditions

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Organometallic chemistry of amidate complexes. accelerating effect of bidentate ligands on the reductive elimination of N-aryl amidates from palladium(II)

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pd-catalyzed alpha-arylation of trimethylsilyl enol ethers with aryl bromides and chlorides: a synergistic effect of two metal fluorides as additives

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palladium-catalyzed coupling of ammonia and lithium amide with aryl halides

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly efficient and functional-group-tolerant catalysts for the palladium-catalyzed coupling of aryl chlorides with thiols

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selective palladium-catalyzed arylation of ammonia: synthesis of anilines as well as symmetrical and unsymmetrical di- and triarylamines

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alpha-arylation of esters catalyzed by the Pd(I) dimer {[P(t-Bu)3]PdBr}2

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palladium-catalyzed alpha-arylation of esters with chloroarenes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transition Metal Catalyzed Synthesis of Arylamines and Aryl Ethers from Aryl Halides and Triflates: Scope and Mechanism

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18681463

retrieved

12 December 2020

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Identifiers

DOI

10.1021/AR800098P

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Fatcat

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https://api.fatcat.wiki/v0/release/oxpmdrpe2fbqbe57jp27qf4rwe

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30 July 2022

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Fatcat ID

release_oxpmdrpe2fbqbe57jp27qf4rwe

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Fatcat

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https://api.fatcat.wiki/v0/release/oxpmdrpe2fbqbe57jp27qf4rwe

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30 July 2022

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OpenCitations bibliographic resource ID

4145801

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4145801

PMC publication ID

2819174

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Fatcat

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https://api.fatcat.wiki/v0/release/oxpmdrpe2fbqbe57jp27qf4rwe

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30 July 2022

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PubMed publication ID

18681463

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Fatcat

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https://api.fatcat.wiki/v0/release/oxpmdrpe2fbqbe57jp27qf4rwe

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30 July 2022

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ResearchGate publication ID

23150510

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