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Angewandte Chemie - International Edition

Volumn 52, Issue 16, 2013, Pages 4453-4456

Direct functionalization of tetrahydrofuran and 1,4-dioxane: Nickel-catalyzed oxidative C(sp3)-H arylation

(4) Liu, Dong a Liu, Chao a Li, Heng a Lei, Aiwen a,b

a WUHAN UNIVERSITY (China)

b LANZHOU INSTITUTE OF CHEMICAL PHYSICS (China)

Author keywords

C H functionalization; nickel; oxidative coupling; radical reactions; tetrahydrofuran

Indexed keywords

ARYLBORONIC ACIDS; C-H FUNCTIONALIZATION; ETHER DERIVATIVES; FUNCTIONALIZATIONS; OXIDATIVE ARYLATION; OXIDATIVE COUPLINGS; RADICAL REACTIONS; TETRA-HYDROFURAN;

AROMATIC COMPOUNDS; CATALYSIS; ETHERS; FUNCTIONAL GROUPS; REACTION KINETICS;

NICKEL;

1,4-DIOXANE; DIOXANE; DIOXANE DERIVATIVE; FURAN DERIVATIVE; NICKEL; TETRAHYDROFURAN;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; OXIDATION REDUCTION REACTION;

CATALYSIS; DIOXANES; FURANS; MOLECULAR STRUCTURE; NICKEL; OXIDATION-REDUCTION;

EID: 84876252727 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201300459 Document Type: Article

Times cited : (271)

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