A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides (Q37356701)

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scientific article published on 18 September 2008

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English	A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides	scientific article published on 18 September 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Stephen L. Buchwald

4

object named as

Stephen L Buchwald

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

author name string

Brett P Fors

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Donald A Watson

2

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Europe PubMed Central

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19 August 2017

Mark R Biscoe

3

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Europe PubMed Central

PMC publication ID

19 August 2017

language of work or name

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publication date

18 September 2008

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Europe PubMed Central

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19 August 2017

Journal of the American Chemical Society

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19 August 2017

130

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Europe PubMed Central

PMC publication ID

19 August 2017

41

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

13552-13554

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Water-mediated catalyst preactivation: an efficient protocol for C-N cross-coupling reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2748321

6 September 2017

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=2748321

6 September 2017

Pd-catalyzed amidation of aryl chlorides using monodentate biaryl phosphine ligands: a kinetic, computational, and synthetic investigation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2748321

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2748321

6 September 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=2748321

6 September 2017

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=2748321

6 September 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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2748321

26 June 2018

Palladium-catalyzed amination of aryl mesylates.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2748321

2 September 2018

Palladium-catalyzed carbonylation of aryl tosylates and mesylates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2748321

2 September 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=2748321

2 September 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=2748321

2 September 2018

NiCl(2)(dppe)-catalyzed cross-coupling of aryl mesylates, arenesulfonates, and halides with arylboronic acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2748321

2 September 2018

Palladium-catalyzed amination of aryl nonaflates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2748321

2 September 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=2748321

2 September 2018

Palladium-Mediated N-Arylation of Heterocyclic Diamines: Insights into the Origin of an Unusual Chemoselectivity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2748321

3 December 2018

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/18798626

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/18798626

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electronic effects on the selectivity of pd-catalyzed C-N bond-forming reactions using biarylphosphine ligands: the competitive roles of amine binding and acidity

1 reference

https://pubmed.ncbi.nlm.nih.gov/18798626

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA8055358

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

ResearchGate publication ID

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