(Q42919758)

English

A general, efficient, and functional-group-tolerant catalyst system for the palladium-catalyzed thioetherification of aryl bromides and iodides

scientific article published on February 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 November 2017

A general, efficient, and functional-group-tolerant catalyst system for the palladium-catalyzed thioetherification of aryl bromides and iodides (English)

1 reference

Europe PubMed Central

PMC publication ID

11 November 2017

1 reference

based on heuristic

inferred from title

John F. Hartwig

2

object named as

John F Hartwig

1 reference

Europe PubMed Central

11 November 2017

PMC publication ID

author name string

Manuel A Fernández-Rodríguez

1

1 reference

Europe PubMed Central

PMC publication ID

11 November 2017

language of work or name

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publication date

1 February 2009

1 reference

Europe PubMed Central

PMC publication ID

11 November 2017

Journal of Organic Chemistry

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Europe PubMed Central

PMC publication ID

11 November 2017

74

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Europe PubMed Central

PMC publication ID

11 November 2017

4

1 reference

Europe PubMed Central

PMC publication ID

11 November 2017

1663-1672

1 reference

Europe PubMed Central

PMC publication ID

11 November 2017

Palladium-catalyzed amination of aryl and heteroaryl 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=2819531

27 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2819531

27 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2819531

27 May 2018

New arylthioindoles: potent inhibitors of tubulin polymerization. 2. Structure-activity relationships and molecular modeling studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2819531

27 May 2018

Arylthioindoles, potent inhibitors of tubulin polymerization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2819531

27 May 2018

Modern Synthetic Methods for Copper-Mediated C(aryl)–O, C(aryl)–N, and C(aryl)–S Bond Formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2819531

27 May 2018

Aryl-aryl bond formation one century after the discovery of the Ullmann reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2819531

27 May 2018

Novel p-arylthio cinnamides as antagonists of leukocyte function-associated antigen-1/intracellular adhesion molecule-1 interaction. 2. Mechanism of inhibition and structure-based improvement of pharmaceutical properties

1 reference

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27 May 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=2819531

16 August 2018

Discovery of novel phenolic antioxidants as inhibitors of vascular cell adhesion molecule-1 expression for use in chronic inflammatory diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2819531

16 August 2018

Iron-Catalyzed S-Arylation of Thiols with Aryl Iodides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2819531

1 December 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19154131

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/19154131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly active, air-stable versatile palladium catalysts for the C-C, C-N, and C-S bond formations via cross-coupling reactions of aryl chlorides

1 reference

https://pubmed.ncbi.nlm.nih.gov/19154131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metal-catalyzed carbon-sulfur bond formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19154131

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/19154131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A general palladium-catalyzed coupling of aryl bromides/triflates and thiols

1 reference

https://pubmed.ncbi.nlm.nih.gov/19154131

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

https://pubmed.ncbi.nlm.nih.gov/19154131

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

https://pubmed.ncbi.nlm.nih.gov/19154131

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

https://pubmed.ncbi.nlm.nih.gov/19154131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cobalt-catalyzed aryl-sulfur bond formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19154131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palladium-catalyzed coupling of ammonia and hydroxide with aryl halides: the direct synthesis of primary anilines and phenols

1 reference

https://pubmed.ncbi.nlm.nih.gov/19154131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simple and Efficient Recyclable Catalytic System for Performing Copper-Catalysed S-Arylation Reactions in the Presence of Water

1 reference

https://pubmed.ncbi.nlm.nih.gov/19154131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The First N-Heterocyclic Carbene-Based Nickel Catalyst for C−S Coupling

1 reference

https://pubmed.ncbi.nlm.nih.gov/19154131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[(CyPF-(t)Bu)PdCl2]: an air-stable, one-component, highly efficient catalyst for amination of heteroaryl and aryl halides

1 reference

https://pubmed.ncbi.nlm.nih.gov/19154131

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19154131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JO802594D

1 reference

Europe PubMed Central

PMC publication ID

11 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 November 2017

ResearchGate publication ID

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