A new class of easily activated palladium precatalysts for facile C-N cross-coupling reactions and the low temperature oxidative addition of aryl chlorides (Q36982977)

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scientific article published on May 2008

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English	A new class of easily activated palladium precatalysts for facile C-N cross-coupling reactions and the low temperature oxidative addition of aryl chlorides	scientific article published on May 2008

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scholarly article

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Europe PubMed Central

PMC publication ID

2587037

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17 August 2017

title

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

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Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

main subject

palladium

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inferred from title

author

Stephen L. Buchwald

series ordinal

3

object named as

Stephen L Buchwald

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stated in

Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

author name string

Mark R Biscoe

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1

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stated in

Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

Brett P Fors

series ordinal

2

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stated in

Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

language of work or name

English

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publication date

1 May 2008

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Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

published in

Journal of the American Chemical Society

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stated in

Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

volume

130

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stated in

Europe PubMed Central

PMC publication ID

2587037

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17 August 2017

issue

21

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Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

page(s)

6686-6687

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Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

cites work

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587037

retrieved

29 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

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587037

retrieved

29 September 2017

An extremely active catalyst for the Negishi cross-coupling reaction

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587037

retrieved

4 September 2018

Pd-Catalyzed Kumada−Corriu Cross-Coupling Reactions at Low Temperatures Allow the Use of Knochel-type Grignard Reagents

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587037

retrieved

4 December 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2587037

retrieved

4 December 2018

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/18447360

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An air and thermally stable one- component catalyst for the amination of aryl chlorides

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18447360

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18447360

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18447360

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

η2-dba Complexes of Pd(0):  The Substituent Effect in Suzuki−Miyaura Coupling

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18447360

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1021/JA801137K

1 reference

stated in

Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

PMC publication ID

2587037

1 reference

stated in

Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

PubMed publication ID

18447360

1 reference

stated in

Europe PubMed Central

PMC publication ID

2587037

retrieved

17 August 2017

ResearchGate publication ID

5405818

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