(Q36078422)

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Nickel-catalyzed cross-coupling of photoredox-generated radicals: uncovering a general manifold for stereoconvergence in nickel-catalyzed cross-couplings

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Nickel-catalyzed cross-coupling of photoredox-generated radicals: uncovering a general manifold for stereoconvergence in nickel-catalyzed cross-couplings (English)

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

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Gary A. Molander

4

object named as

Gary A Molander

1 reference

Europe PubMed Central

12 August 2017

PMC publication ID

Marisa C. Kozlowski

5

object named as

Marisa C Kozlowski

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

author name string

Osvaldo Gutierrez

1

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

John C Tellis

2

1 reference

Europe PubMed Central

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12 August 2017

David N Primer

3

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Europe PubMed Central

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12 August 2017

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publication date

8 April 2015

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Europe PubMed Central

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12 August 2017

Journal of the American Chemical Society

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Europe PubMed Central

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12 August 2017

137

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Europe PubMed Central

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12 August 2017

15

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

4896-4899

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Nickel-catalyzed Negishi arylations of propargylic bromides: a mechanistic investigation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Nickel-catalyzed asymmetric reductive cross-coupling between vinyl and benzyl electrophiles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Stereospecific pd-catalyzed cross-coupling reactions of secondary alkylboron nucleophiles and aryl chlorides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Dual catalysis. Merging photoredox with nickel catalysis: coupling of α-carboxyl sp³-carbons with aryl halides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Dual catalysis. Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Recent advances in homogeneous nickel catalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Causation in a cascade: the origins of selectivities in intramolecular nitrone cycloadditions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Catalytic Asymmetric γ-Alkylation of Carbonyl Compounds via Stereoconvergent Suzuki Cross-Couplings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Stereoconvergent Amine-Directed Alkyl–Alkyl Suzuki Reactions of Unactivated Secondary Alkyl Chlorides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Asymmetric alkyl-alkyl cross-couplings of unactivated secondary alkyl electrophiles: stereoconvergent Suzuki reactions of racemic acylated halohydrins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Nature of intermediates in organo-SOMO catalysis of alpha-arylation of aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Secondary alkyl halides in transition-metal-catalyzed cross-coupling reactions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

2 October 2017

Single-electron transmetalation: an enabling technology for secondary alkylboron cross-coupling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

11 July 2018

Access to Formally Ni(I) States in a Heterobimetallic NiZn System

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

11 July 2018

Catalytic asymmetric reductive acyl cross-coupling: synthesis of enantioenriched acyclic α,α-disubstituted ketones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

11 July 2018

Density functional theory studies of negishi alkyl-alkyl cross-coupling reactions catalyzed by a methylterpyridyl-Ni(I) complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

11 July 2018

Enantioselective alkyl-alkyl Suzuki cross-couplings of unactivated homobenzylic halides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4576934

23 September 2018

Theoretical study on the mechanism of Ni-catalyzed alkyl-alkyl Suzuki cross-coupling

1 reference

https://pubmed.ncbi.nlm.nih.gov/25836634

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stereospecific Couplings of Secondary and Tertiary Boronic Esters

1 reference

https://pubmed.ncbi.nlm.nih.gov/25836634

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stereoretentive Pd-catalysed Stille cross-coupling reactions of secondary alkyl azastannatranes and aryl halides

1 reference

https://pubmed.ncbi.nlm.nih.gov/25836634

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficient synthesis of secondary alkyl fluorides via Suzuki cross-coupling reaction of 1-halo-1-fluoroalkanes

1 reference

https://pubmed.ncbi.nlm.nih.gov/25836634

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[CpNi(dithiolene)] (and diselenolene) neutral radical complexes

1 reference

https://pubmed.ncbi.nlm.nih.gov/25836634

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ligand redox effects in the synthesis, electronic structure, and reactivity of an alkyl-alkyl cross-coupling catalyst

1 reference

https://pubmed.ncbi.nlm.nih.gov/25836634

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Self-control tames the coupling of reactive radicals

1 reference

https://pubmed.ncbi.nlm.nih.gov/25836634

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA513079R

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

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