Cross-dehydrogenative coupling and oxidative-amination reactions of ethers and alcohols with aromatics and heteroaromatics.

about

Copper-Catalyzed Syntheses of Pyrene-Pyrazole Pharmacophores and Structure Activity Studies for Tubulin Polymerization tert-Butyl peroxybenzoate mediated formation of 3-alkylated quinolines from N-propargylamines via a cascade radical addition/cyclization reaction

P2860

Q58125217-B9A8869C-744F-439C-A212-75DDCB882053 Q58623750-522542B9-BBF1-46A0-9F06-6B591547B3D8

P2860

Cross-dehydrogenative coupling and oxidative-amination reactions of ethers and alcohols with aromatics and heteroaromatics.

Item

http://www.wikidata.org/entity/Q42130713

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Cross-dehydrogenative coupling ...... aromatics and heteroaromatics.

@en

Cross-dehydrogenative coupling ...... aromatics and heteroaromatics.

@nl

type

Item

label

Cross-dehydrogenative coupling ...... aromatics and heteroaromatics.

@en

Cross-dehydrogenative coupling ...... aromatics and heteroaromatics.

@nl

prefLabel

Cross-dehydrogenative coupling ...... aromatics and heteroaromatics.

@en

Cross-dehydrogenative coupling ...... aromatics and heteroaromatics.

@nl

P1476

Cross-dehydrogenative coupling ...... aromatics and heteroaromatics

@en

P2093

Prasanna K Vuram

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

P2860

A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes

Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides.

Asymmetric cross-dehydrogenative coupling enabled by the design and application of chiral triazole-containing phosphoric acids.

Direct evidence of a dinuclear copper intermediate in Cu(I)-catalyzed azide-alkyne cycloadditions

Ruthenium-Catalyzed C-H Bond Activation Approach to Azolyl Aminals and Hemiaminal Ethers, Mechanistic Evaluations, and Isomer Interconversion.

Iron(III) chloride in oxidative C-C coupling reactions.

Beyond traditional cross couplings: the scope of the cross dehydrogenative coupling reaction.

Intermolecular oxidative cross-coupling of arenes.

Direct C-H transformation via iron catalysis.

Direct Sp3α-C-H activation and functionalization of alcohol and ether.

P304

5845-5888

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

P31

scholarly article

P356

10.1039/C7SC01045A

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

P433

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

P478

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

P50

Mahesh K Lakshman

P577

2017-06-30T00:00:00Z

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

P698

28970941

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

P932

5618789

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

Cross-dehydrogenative coupling and oxidative-amination reactions of ethers and alcohols with aromatics and heteroaromatics.

about

P2860

P2860

Cross-dehydrogenative coupling and oxidative-amination reactions of ethers and alcohols with aromatics and heteroaromatics.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932