Cross coupling: When is free really free? (Q42792472)

From Wikidata

Jump to navigation Jump to search

scientific article published on 7 November 2010

Language	Label	Description	Also known as
English	Cross coupling: When is free really free?	scientific article published on 7 November 2010

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 November 2017

Cross coupling: When is free really free? (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 November 2017

Nicholas E. Leadbeater

object named as

Nicholas E Leadbeater

1

0 references

publication date

7 November 2010

1 reference

Europe PubMed Central

PubMed publication ID

7 November 2017

Nature Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

7 November 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

7 November 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

7 November 2017

1007-1009

1 reference

Europe PubMed Central

PubMed publication ID

7 November 2017

An efficient organocatalytic method for constructing biaryls through aromatic C-H activation

1 reference

https://api.crossref.org/works/10.1038%2FNCHEM.913

21 January 2018

Transition-Metal-Free Suzuki-Type Coupling Reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107360

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Coupling of nitrogen heteroaromatics and alkanes without transition metals: a new oxidative cross-coupling at C-H/C-H bonds

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107360

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unlikeliness of Pd-Free Gold(I)-Catalyzed Sonogashira Coupling Reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107360

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Organocatalysis in cross-coupling: DMEDA-catalyzed direct C-H arylation of unactivated benzene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107360

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Potassium t-butoxide alone can promote the biaryl coupling of electron-deficient nitrogen heterocycles and haloarenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107360

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transition-metal-free Suzuki-type coupling reactions: scope and limitations of the methodology

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107360

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iron-catalyzed direct arylation through an aryl radical transfer pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107360

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First Examples of Transition-Metal Free Sonogashira-Type Couplings

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107360

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid and amenable suzuki coupling reaction in water using microwave and conventional heating

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107360

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the role of metal contaminants in catalyses with FeCl3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107360

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/NCHEM.913

1 reference

Europe PubMed Central

PubMed publication ID

7 November 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 November 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q42792472&oldid=2205650263"