t-BuONa-mediated direct C-H halogenation of electron-deficient (hetero)arenes.

about

t-BuONa-mediated direct C-H halogenation of electron-deficient (hetero)arenes.

Item

http://www.wikidata.org/entity/Q48230890

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

t-BuONa-mediated direct C-H halogenation of electron-deficient (hetero)arenes.

@en

t-BuONa-mediated direct C-H halogenation of electron-deficient

@nl

type

Item

label

t-BuONa-mediated direct C-H halogenation of electron-deficient (hetero)arenes.

@en

t-BuONa-mediated direct C-H halogenation of electron-deficient

@nl

prefLabel

t-BuONa-mediated direct C-H halogenation of electron-deficient (hetero)arenes.

@en

t-BuONa-mediated direct C-H halogenation of electron-deficient

@nl

P1476

t-BuONa-mediated direct C-H halogenation of electron-deficient (hetero)arenes.

@en

P2093

Xia Liu

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

Xin Zhao

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

P2860

Silylation of C–H bonds in aromatic heterocycles by an Earth-abundant metal catalyst

A general method for copper-catalyzed arene cross-dimerization

Regioselective (site-selective) functionalization of unsaturated halogenated nitrogen, oxygen and sulfur heterocycles by Pd-catalysed cross-couplings and direct arylation processes.

Transition-Metal-Free C3 Arylation of Indoles with Aryl Halides.

KOtBu: A Privileged Reagent for Electron Transfer Reactions?

Access to a new class of synthetic building blocks via trifluoromethoxylation of pyridines and pyrimidines.

In situ generation and trapping of aryllithium and arylpotassium species by halogen, sulfur, and carbon electrophiles.

A simple base-mediated halogenation of acidic sp2 C-H bonds under noncryogenic conditions.

An efficient organocatalytic method for constructing biaryls through aromatic C-H activation.

Oxidative dimerization of (hetero)aromatic amines utilizing t-BuOI leading to (hetero)aromatic azo compounds: scope and mechanistic studies.

P304

886-890

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

P31

scholarly article

P356

10.1039/C7OB03081A

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

P433

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

P478

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

P50

Fushun Liang

Bao-Yi Ren

P577

2018-01-17T00:00:00Z

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

P698

29340407

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