[Cp*RhCl2]2-catalyzed ortho-C-H bond amination of acetophenone o-methyloximes with primary N-chloroalkylamines: convenient synthesis of N-alkyl-2-acylanilines (Q44387453)

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scientific article published in August 2013

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English	[Cp*RhCl2]2-catalyzed ortho-C-H bond amination of acetophenone o-methyloximes with primary N-chloroalkylamines: convenient synthesis of N-alkyl-2-acylanilines	scientific article published in August 2013

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scholarly article

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Europe PubMed Central

PubMed publication ID

2 December 2017

[Cp*RhCl2]2-catalyzed ortho-C-H bond amination of acetophenone o-methyloximes with primary N-chloroalkylamines: convenient synthesis of N-alkyl-2-acylanilines (English)

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Europe PubMed Central

PubMed publication ID

2 December 2017

author name string

Ka-Ho Ng

1

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2 December 2017

Zhongyuan Zhou

2

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2 December 2017

Wing-Yiu Yu

3

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2 December 2017

language of work or name

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publication date

1 August 2013

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2 December 2017

Chemical Communications

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2 December 2017

49

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2 December 2017

63

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2 December 2017

7031-7033

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PubMed publication ID

2 December 2017

Towards mild metal-catalyzed C-H bond activation

1 reference

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Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

1 reference

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Catalytic C-H amination: recent progress and future directions

1 reference

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Palladium-catalyzed amination of aromatic C-H bonds with oxime esters

1 reference

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Pd(II)-catalyzed amination of C-H bonds using single-electron or two-electron oxidants.

1 reference

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Oxidative Pd(II)-catalyzed C-H bond amination to carbazole at ambient temperature

1 reference

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Synthesis of beta-, gamma-, and delta-lactams via Pd(II)-catalyzed C-H activation reactions

1 reference

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Synthesis of indolines and tetrahydroisoquinolines from arylethylamines by Pd(II)-catalyzed C-H activation reactions

1 reference

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Intermolecular Amidation of Unactivated sp2and sp3C−H Bonds via Palladium-Catalyzed Cascade C−H Activation/Nitrene Insertion

1 reference

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Pd-catalyzed ortho-C-H acylation/cross coupling of aryl ketone O-methyl oximes with aldehydes using tert-butyl hydroperoxide as oxidant.

1 reference

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Palladium-catalyzed oxidative ethoxycarbonylation of aromatic C-H bond with diethyl azodicarboxylate

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Copper-mediated amidation of heterocyclic and aromatic C-H bonds

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Organocatalytic, oxidative, intermolecular amination and hydrazination of simple arenes at ambient temperature.

1 reference

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Metal-Free Intermolecular Oxidative C–N Bond Formation via Tandem C–H and N–H Bond Functionalization

1 reference

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Pd-Catalyzed Intermolecular C–H Amination with Alkylamines

1 reference

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C-C, C-O and C-N bond formation via rhodium(III)-catalyzed oxidative C-H activation.

1 reference

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Rhodium-catalyzed C-C bond formation via heteroatom-directed C-H bond activation

1 reference

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Oxidative coupling of aromatic substrates with alkynes and alkenes under rhodium catalysis.

1 reference

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Rhodium(III)-catalyzed indazole synthesis by C-H bond functionalization and cyclative capture

1 reference

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Mild rhodium(III)-catalyzed cyclization of amides with α,β-unsaturated aldehydes and ketones to azepinones: application to the synthesis of the homoprotoberberine framework

1 reference

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21 January 2018

Rhodium-catalyzed direct C-H amination of benzamides with aryl azides: a synthetic route to diarylamines.

1 reference

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21 January 2018

Electrophilic amination of carbanions

1 reference

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21 January 2018

Chemistry of N-bromamines and N-chloramines

1 reference

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21 January 2018

Recent advances in the solid-phase combinatorial synthetic strategies for the quinoxaline, quinazoline and benzimidazole based privileged structures

1 reference

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21 January 2018

The combinatorial synthesis of bicyclic privileged structures or privileged substructures.

1 reference

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21 January 2018

Rh[III]-Catalyzed Direct C–H Amination Using N-Chloroamines at Room Temperature

1 reference

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21 January 2018

Identifiers

10.1039/C3CC42937G

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

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