(Q24650794)

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Alkyl-alkyl suzuki cross-couplings of unactivated secondary alkyl halides at room temperature

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Alkyl-alkyl suzuki cross-couplings of unactivated secondary alkyl halides at room temperature (English)

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Bunnai Saito

1

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Gregory C Fu

series ordinal

2

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language of work or name

English

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publication date

8 August 2007

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published in

Journal of the American Chemical Society

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volume

129

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issue

31

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page(s)

9602-3

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cites work

Catalysts for Cross-Coupling Reactions with Non-activated Alkyl Halides

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569998

retrieved

7 April 2017

Alkylboranes in the Suzuki-Miyaura Coupling: Stereochemical and Mechanistic Studies

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2569998

retrieved

28 September 2017

Amino alcohols as ligands for nickel-catalyzed suzuki reactions of unactivated alkyl halides, including secondary alkyl chlorides, with arylboronic acids

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17628067

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12 December 2020

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Cross-couplings of unactivated secondary alkyl halides: room-temperature nickel-catalyzed Negishi reactions of alkyl bromides and iodides

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17628067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suzuki cross-couplings of unactivated secondary alkyl bromides and iodides

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17628067

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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PubMed publication ID

17628067

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ResearchGate publication ID

6210284

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(Q24650794)

Alkyl-alkyl suzuki cross-couplings of unactivated secondary alkyl halides at room temperature

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