(Q37014864)

English

Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions

scientific article published on December 2006

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions (English)

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

1 reference

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author name string

Kyung Soo Yoo

1

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Cheol Hwan Yoon

2

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Rajesh K Mishra

3

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Young Chun Jung

4

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Sung Wook Yi

5

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Kyung Woon Jung

6

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

language of work or name

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publication date

1 December 2006

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Journal of the American Chemical Society

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Europe PubMed Central

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17 August 2017

128

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Europe PubMed Central

PMC publication ID

17 August 2017

50

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

16384-16393

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Vinylic tellurides: from preparation to their applicability in organic synthesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

29 September 2017

Palladium oxidase catalysis: selective oxidation of organic chemicals by direct dioxygen-coupled turnover

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

29 September 2017

The first ligand-modulated oxidative Heck vinylation. Efficient catalysis with molecular oxygen as palladium(0) oxidant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

29 September 2017

The heck reaction as a sharpening stone of palladium catalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

29 September 2017

Highly regioselective palladium-catalyzed beta-arylation of N, N-dialkylallylamines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

29 September 2017

Mechanistic study of alcohol oxidation by the Pd(OAc)(2)/O(2)/DMSO catalyst system and implications for the development of improved aerobic oxidation catalysts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

27 June 2018

Expanding organoboron chemistry: epoxidation of potassium organotrifluoroborates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

4 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=2602842

4 September 2018

Electronic control of the regiochemistry in the Heck reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

4 September 2018

Synthetic applications of o- and p-halobenzyl sulfones as zwitterionic synthons: preparation of ortho-substituted cinnamates and biarylacetic acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

4 September 2018

The palladium-catalyzed oxidative kinetic resolution of secondary alcohols with molecular oxygen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

4 September 2018

Screening of homogeneous catalysts by fluorescence resonance energy transfer. Identification of catalysts for room-temperature Heck reactions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

4 September 2018

Mechanism of the Palladium-Catalyzed Homocoupling of Arylboronic Acids: Key Involvement of a Palladium Peroxo Complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2602842

4 December 2018

Oxygenation of nitrogen-coordinated palladium(0): synthetic, structural, and mechanistic studies and implications for aerobic oxidation catalysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oxygen-promoted palladium(II) catalysis: facile C(sp2)-C(sp2) bond formation via cross-coupling of alkenylboronic compounds and olefins

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Green, catalytic oxidation of alcohols in water

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preparation of enamides via palladium-catalyzed amidation of enol tosylates

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mizoroki-Heck type reaction of organoboron reagents with alkenes and alkynes. A Pd(II)-catalyzed pathway with Cu(OAc)2 as an oxidant

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mild and efficient aryl-alkenyl coupling via Pd(II) catalysis in the presence of oxygen or Cu(II) oxidants

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toward waste-free production of Heck products with a catalytic palladium system under oxygen

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oxygen-promoted Pd(II) catalysis for the coupling of organoboron compounds and olefins

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palladium-catalyzed enantioselective oxidations of alcohols using molecular oxygen

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regioselective Heck couplings of alpha,beta-unsaturated tosylates and mesylates with electron-rich olefins

1 reference

https://pubmed.ncbi.nlm.nih.gov/17165795

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA063710Z

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

release_g4twfi4aprbnrbosv7a7xzn3ze

1 reference

https://api.fatcat.wiki/v0/release/g4twfi4aprbnrbosv7a7xzn3ze

24 November 2022

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mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

ResearchGate publication ID

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