(Q34264792)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22463689%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

title

Replacing conventional carbon nucleophiles with electrophiles: nickel-catalyzed reductive alkylation of aryl bromides and chlorides (English)

1 reference

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27 January 2020

0 references

1 reference

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27 January 2020

Daniel A Everson

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22463689%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Brittany A Jones

series ordinal

1 reference

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27 January 2020

language of work or name

English

0 references

publication date

30 March 2012

1 reference

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Journal of the American Chemical Society

27 January 2020

published in

1 reference

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27 January 2020

volume

134

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27 January 2020

issue

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27 January 2020

page(s)

6146-6159

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22463689%20AND%20SRC:MED&resulttype=core&format=json

The medicinal chemist's toolbox: an analysis of reactions used in the pursuit of drug candidates.

27 January 2020

cites work

1 reference

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“On water” sp3–sp2 cross-couplings between benzylic and alkenyl halides

6 July 2018

1 reference

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Structure-based design, synthesis and preliminary anti-inflammatory activity of bolinaquinone analogues

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Nickel-catalyzed cross-couplings involving carbon-oxygen bonds

6 July 2018

1 reference

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Palladium-Catalyzed, Direct Boronic Acid Synthesis from Aryl Chlorides: A Simplified Route to Diverse Boronate Ester Derivatives

6 July 2018

1 reference

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Nickel-Catalyzed Cross-Coupling of Potassium Aryl- and Heteroaryltrifluoroborates with Unactivated Alkyl Halides

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Factors determining the selection of organic reactions by medicinal chemists and the use of these reactions in arrays (small focused libraries).

6 July 2018

1 reference

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Cross-couplings between benzylic and aryl halides "on water": synthesis of diarylmethanes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Zn-mediated, Pd-catalyzed cross-couplings in water at room temperature without prior formation of organozinc reagents

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Cross-coupling reactions of aromatic and heteroaromatic silanolates with aromatic and heteroaromatic halides

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

An improved protocol for the Pd-catalyzed alpha-arylation of aldehydes with aryl halides.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

One-pot Negishi cross-coupling reactions of in situ generated zinc reagents with aryl chlorides, bromides, and triflates

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

A new class of easily activated palladium precatalysts for facile C-N cross-coupling reactions and the low temperature oxidative addition of aryl chlorides

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

DirectedorthoMetalation−Boronation and Suzuki−Miyaura Cross Coupling of Pyridine Derivatives: A One-Pot Protocol to Substituted Azabiaryls#

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Organotrifluoroborates: protected boronic acids that expand the versatility of the Suzuki coupling reaction

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Analysis of the reactions used for the preparation of drug candidate molecules

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Microwave-assisted Suzuki coupling reactions with an encapsulated palladium catalyst for batch and continuous-flow transformations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Reaction progress kinetic analysis: a powerful methodology for mechanistic studies of complex catalytic reactions

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Highly efficient, general procedure for the preparation of alkylzinc reagents from unactivated alkyl bromides and chlorides

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Aryl-aryl bond formation one century after the discovery of the Ullmann reaction

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Nickel-catalyzed, sodium iodide-promoted reductive dimerization of alkyl halides, alkyl pseudohalides, and allylic acetates

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Neopentylglycolborylation of aryl mesylates and tosylates catalyzed by Ni-based mixed-ligand systems activated with Zn.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Suzuki-Miyaura coupling of aryl carbamates, carbonates, and sulfamates

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Functional group tolerant Kumada-Corriu-Tamao coupling of nonactivated alkyl halides with aryl and heteroaryl nucleophiles: catalysis by a nickel pincer complex permits the coupling of functionalized Grignard reagents.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Cobalt-catalyzed cross-coupling between in situ prepared arylzinc halides and 2-chloropyrimidine or 2-chloropyrazine

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Synthesis of functionalised diarylmethanes via a cobalt-catalysed cross-coupling of arylzinc species with benzyl chlorides

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Biaryl construction via Ni-catalyzed C-O activation of phenolic carboxylates

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Cross-coupling reactions of aryl pivalates with boronic acids

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Multistep synthesis of complex boronic acids from simple MIDA boronates

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Negishi cross-couplings of unsaturated halides bearing relatively acidic hydrogen atoms with organozinc reagents.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Differentially protected benzenediboronic acids: divalent cross-coupling modules for the efficient synthesis of boron-substituted oligoarenes

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

A silicon-based approach to oligoarenes by iterative cross-coupling reactions of halogenated organo[(2-hydroxymethyl)phenyl]dimethylsilanes

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Hiyama Reactions of Activated and Unactivated Secondary Alkyl Halides Catalyzed by a Nickel/Norephedrine Complex

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Boron-masking strategy for the selective synthesis of oligoarenes via iterative Suzuki-Miyaura coupling

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Stille cross-couplings of unactivated secondary alkyl halides using monoorganotin reagents

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

A modular synthesis of the lamellarins: total synthesis of lamellarin G trimethyl ether.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

New chemical synthesis of functionalized arylzinc compounds from aromatic or thienyl bromides under mild conditions using a simple cobalt catalyst and zinc dust

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Cobalt-catalyzed direct electrochemical cross-coupling between aryl or heteroaryl halides and allylic acetates or carbonates

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Comparative QSAR: Radical Reactions of Benzene Derivatives in Chemistry and Biology.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Mechanism of the Heck reaction using a phosphapalladacycle as the catalyst: classical versus palladium(IV) intermediates

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Heterocyclization by catalytic carbonickelation of alkynes: a domino sequence involving vinylnickels

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324882

Palladium-catalyzed alpha-arylation of aldehydes with bromo- and chloroarenes catalyzed by [{Pd(allyl)Cl}2] and dppf or Q-phos

28 October 2018

1 reference

12 December 2020

Nickel-Catalyzed Direct Electrochemical Cross-Coupling between Aryl Halides and Activated Alkyl Halides

1 reference

12 December 2020

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

1 reference

12 December 2020

Novel Rh catalysis in cross-coupling between alkyl halides and arylzinc compounds possessing ortho-COX (X = OR, NMe2, or Ph) groups

1 reference

12 December 2020

Reductive conjugate addition of haloalkanes to enones to form silyl enol ethers

1 reference

12 December 2020

Direct method for carbon-carbon bond formation: the functional group tolerant cobalt-catalyzed alkylation of aryl halides

1 reference

12 December 2020

Directed ortho-metalation of unprotected benzoic acids. Methodology and regioselective synthesis of useful contiguously 3- and 6-substituted 2-methoxybenzoic acid building blocks

1 reference

12 December 2020

Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Alkyl Halides

1 reference

12 December 2020

Asymmetric Induction in the Electrochemical Cross-Coupling of Aryl Halides with alpha-Chloropropionic Acid Derivatives Catalyzed by Nickel Complexes

1 reference

12 December 2020

High affinity retinoic acid receptor antagonists: analogs of AGN 193109

1 reference

12 December 2020

A novel, chemoselective and efficient microwave-assisted deprotection of silyl ethers with selectfluor

1 reference

12 December 2020

Neopentylglycolborylation of Aryl Chlorides Catalyzed by the Mixed Ligand System NiCl2(dppp)/dppf

1 reference

12 December 2020

Domino iron catalysis: direct aryl-alkyl cross-coupling

1 reference

12 December 2020

Synthesis of Biaryls via a Nickel(0)-Catalyzed Cross-Coupling Reaction of Chloroarenes with Arylboronic Acids

1 reference

12 December 2020

C−H Activation for the Construction of C−B Bonds

1 reference

12 December 2020

Nickel-Catalyzed Cross-Couplings of Organosilicon Reagents with Unactivated Secondary Alkyl Bromides

1 reference

12 December 2020

Iridium-Catalyzed CH Activation versus DirectedorthoMetalation: Complementary Borylation of Aromatics and Heteroaromatics

1 reference

12 December 2020

Palladium-catalyzed tetrakis(dimethylamino)ethylene-promoted reductive coupling of aryl halides

1 reference

12 December 2020

A general method for the direct alpha-arylation of aldehydes with aryl bromides and chlorides

1 reference

12 December 2020

Nickel-Catalyzed Cross-Coupling of Non-activated and Functionalized Alkyl Halides with Alkyl Grignard Reagents

1 reference

12 December 2020

High temperature metalation of functionalized aromatics and heteroaromatics using (tmp)2Zn x 2 MgCl2 x 2 LiCl and microwave irradiation

1 reference

12 December 2020

Nickel-Catalyzed Negishi Cross-Coupling Reactions of Secondary Alkylzinc Halides and Aryl Iodides

1 reference

12 December 2020

Fluorine in medicinal chemistry

1 reference

12 December 2020

New chemical cross-coupling between aryl halides and allylic acetates using a cobalt catalyst

1 reference

12 December 2020

Halide LigandsMore Than Just σ-Donors? A Structural and Spectroscopic Study of Homologous Organonickel Complexes

1 reference

12 December 2020

Palladium-catalyzed borylation of aryl halides or triflates with dialkoxyborane: A novel and facile synthetic route to arylboronates

1 reference

12 December 2020

A Structure–Activity Study of Ni-Catalyzed Alkyl–Alkyl Kumada Coupling. Improved Catalysts for Coupling of Secondary Alkyl Halides

1 reference

12 December 2020

Ueber das Aethyl- und Diäthylbenzol

1 reference

14 September 2024

https://opencitations.net/index/api/v1/citations/10.1002/JLAC.18671440308

Identifiers

DOI

10.1021/JA301769R

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22463689%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22463689%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

PubMed publication ID

22463689

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22463689%20AND%20SRC:MED&resulttype=core&format=json