General allylic C-H alkylation with tertiary nucleophiles. - Wikidata - awgldk - TriplyDB

General allylic C-H alkylation with tertiary nucleophiles.

General allylic C-H alkylation with tertiary nucleophiles.

http://www.wikidata.org/entity/Q39044891

about

The emergence of sulfoxides as efficient ligands in transition metal catalysis.C-H Coupling Reactions Directed by Sulfoxides: Teaching an Old Functional Group New Tricks.Chiral counteranion strategy for asymmetric oxidative C(sp³)-H/C(sp³)-H coupling: enantioselective α-allylation of aldehydes with terminal alkenes.N-Boc amines to oxazolidinones via Pd(II)/bis-sulfoxide/Brønsted acid co-catalyzed allylic C-H oxidation.Metal-free direct alkylation of unfunctionalized allylic/benzylic sp3 C-H bonds via photoredox induced radical cation deprotonation.Palladium-catalyzed C-H activation of N-allyl imines: regioselective allylic alkylations to deliver substituted aza-1,3-dienes.Enantioselective Allylic C-H Oxidation of Terminal Olefins to Isochromans by Palladium(II)/Chiral Sulfoxide Catalysis.Palladium-catalyzed aerobic oxidative double allylic C-H oxygenation of alkenes: a novel and straightforward route to α,β-unsaturated esters.TEMPO-mediated allylic C-H amination with hydrazones.Hydrophenylation of ethylene using a cationic Ru(ii) catalyst: comparison to a neutral Ru(ii) catalyst

P2860

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P2860

General allylic C-H alkylation with tertiary nucleophiles.

http://www.wikidata.org/entity/Q39044891

description

2014 nî lūn-bûn

@nan

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

2014年论文

@zh

2014年论文

@zh-cn

name

General allylic C-H alkylation with tertiary nucleophiles.

@en

General allylic C-H alkylation with tertiary nucleophiles.

@nl

type

label

General allylic C-H alkylation with tertiary nucleophiles.

@en

General allylic C-H alkylation with tertiary nucleophiles.

@nl

prefLabel

General allylic C-H alkylation with tertiary nucleophiles.

@en

General allylic C-H alkylation with tertiary nucleophiles.

@nl

P1433

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P1433

Journal of the American Chemical Society

P1476

General allylic C-H alkylation with tertiary nucleophiles.

@en

P2093

Andrew J Young

http://www.w3.org/2001/XMLSchema#string

Jennifer M Howell

http://www.w3.org/2001/XMLSchema#string

M Christina White

http://www.w3.org/2001/XMLSchema#string

Wei Liu

http://www.w3.org/2001/XMLSchema#string

P2860

Binding and functional selectivity of himbacine for cloned and neuronal muscarinic receptors

Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

Catalytic C–H functionalization by metal carbenoid and nitrenoid insertion

Libraries from natural product-like scaffolds.

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

The Construction of All-Carbon Quaternary Stereocenters by Use of Pd-Catalyzed Asymmetric Allylic Alkylation Reactions in Total Synthesis

Combined effects on selectivity in Fe-catalyzed methylene oxidation.

Molecular complexity via C-H activation: a dehydrogenative Diels-Alder reaction.

A predictably selective aliphatic C-H oxidation reaction for complex molecule synthesis.

Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage.

P304

5750-5754

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scholarly article

P356

10.1021/JA500726E

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15

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136

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2014-04-02T00:00:00Z

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260914276

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24641574

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