Highly reactive, general and long-lived catalysts for palladium-catalyzed amination of heteroaryl and aryl chlorides, bromides, and iodides: scope and structure-activity relationships (Q41768959)

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scientific article published on 30 April 2008

Language	Label	Description	Also known as
English	Highly reactive, general and long-lived catalysts for palladium-catalyzed amination of heteroaryl and aryl chlorides, bromides, and iodides: scope and structure-activity relationships	scientific article published on 30 April 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

9 October 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 (English)

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

John F. Hartwig

3

object named as

John F Hartwig

1 reference

Europe PubMed Central

9 October 2017

PMC publication ID

author name string

Qilong Shen

1

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Tokutaro Ogata

2

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

language of work or name

0 references

publication date

30 April 2008

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Europe PubMed Central

PMC publication ID

9 October 2017

Journal of the American Chemical Society

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Europe PubMed Central

PMC publication ID

9 October 2017

130

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

20

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

6586-6596

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

6 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

6 June 2018

Palladium-catalyzed coupling reactions of aryl chlorides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

6 June 2018

Synthesis of bulky and electron-rich MOP-type ligands and their applications in palladium-catalyzed C-N bond formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

Triazole-based monophosphine ligands for palladium-catalyzed cross-coupling reactions of aryl chlorides.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

Study of a new rate increasing "base effect" in the palladium-catalyzed amination of aryl iodides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

New ligands for a general palladium-catalyzed amination of aryl and heteroaryl chlorides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

Easy access to novel substituted 6-aminoimidazo[1,2-a]pyridines using palladium- and copper-catalyzed aminations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

Scope and mechanism of palladium-catalyzed amination of five-membered heterocyclic halides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

Amination reactions of aryl halides with nitrogen-containing reagents mediated by palladium/imidazolium salt systems

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

High turnover number and rapid, room-temperature amination of chloroarenes using saturated carbene ligands.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

18 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2822544

2 December 2018

Monoligated palladium species as catalysts in cross-coupling reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved method for the palladium-catalyzed amination of aryl iodides

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

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

https://pubmed.ncbi.nlm.nih.gov/18444639

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pd-catalyzed N-arylation of heteroarylamines

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

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

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

(IPr)Pd(acac)Cl: An Easily Synthesized, Efficient, and Versatile Precatalyst for C−N and C−C Bond Formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The First Phosphine Oxide Ligand Precursors for Transition Metal Catalyzed Cross-Coupling Reactions: C-C, C-N, and C-S Bond Formation on Unactivated Aryl Chlorides

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A diaminochlorophosphine for palladium-catalyzed arylations of amines and ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Application of a New Bicyclic Triaminophosphine Ligand in Pd-Catalyzed Buchwald−Hartwig Amination Reactions of Aryl Chlorides, Bromides, and Iodides

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid Room Temperature Buchwald–Hartwig and Suzuki–Miyaura Couplings of Heteroaromatic Compounds Employing Low Catalyst Loadings

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palladium-Catalyzed Intermolecular Coupling of Aryl Chlorides and Sulfonamides under Microwave Irradiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An air-stable palladium/N-heterocyclic carbene complex and its reactivity in aryl amination.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Zinc trimethylsilylamide as a mild ammonia equivalent and base for the amination of aryl halides and triflates

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18444639

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA077074W

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

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