(Q41929605)

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Nickel-catalyzed Mizoroki-Heck reaction of aryl sulfonates and chlorides with electronically unbiased terminal olefins: high selectivity for branched products

scientific article published on 8 January 2014

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Nickel-catalyzed Mizoroki-Heck reaction of aryl sulfonates and chlorides with electronically unbiased terminal olefins: high selectivity for branched products (English)

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

1 reference

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Sarah Z Tasker

1

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Alicia C Gutierrez

2

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Timothy F Jamison

3

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

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publication date

8 January 2014

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Europe PubMed Central

PMC publication ID

14 October 2017

Angewandte Chemie International Edition

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53

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Europe PubMed Central

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14 October 2017

7

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

1858-1861

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Simplifying nickel(0) catalysis: an air-stable nickel precatalyst for the internally selective benzylation of terminal alkenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159703

5 June 2018

Catalyst-controlled regioselectivity in the synthesis of branched conjugated dienes via aerobic oxidative Heck reactions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159703

5 June 2018

Nickel-catalyzed Heck-type reactions of benzyl chlorides and simple olefins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159703

5 June 2018

From α-arylation of olefins to acylation with aldehydes: a journey in regiocontrol of the Heck reaction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159703

5 June 2018

Nickel-catalyzed cross-couplings involving carbon-oxygen bonds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159703

5 June 2018

Nickel-catalyzed allylic substitution of simple alkenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159703

5 June 2018

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=4159703

5 June 2018

Selective arylation and vinylation at the α position of vinylarenes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159703

18 August 2018

Intermolecular Mizoroki-Heck reaction of aliphatic olefins with high selectivity for substitution at the internal position.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159703

18 August 2018

Arylation of Olefin with Aryl Iodide Catalyzed by Palladium

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201308391

21 January 2018

Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201308391

21 January 2018

Mild and efficient nickel-catalyzed Heck reactions with electron-rich olefins

1 reference

https://pubmed.ncbi.nlm.nih.gov/24402966

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nickel(0)-catalyzed Heck cross-coupling via activation of aryl C-OPiv bonds

1 reference

https://pubmed.ncbi.nlm.nih.gov/24402966

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ligand exchange as the first irreversible step in the nickel-catalyzed cross-coupling reaction of Grignard reagents

1 reference

https://pubmed.ncbi.nlm.nih.gov/24402966

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Directed ortho metalation methodology. The N,N-dialkyl aryl O-sulfamate as a new directed metalation group and cross-coupling partner for Grignard reagents

1 reference

https://pubmed.ncbi.nlm.nih.gov/24402966

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/ANIE.201308391

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

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