Copper(I)-Catalyzed Alkyl- and Arylsulfenylation of 3,4-Dihalo-2(5H )-furanones (X=Br, Cl) with Sulfoxides under Mild Conditions-Reference-Cited by-同舟云学术

Copper(I)-Catalyzed Alkyl- and Arylsulfenylation of 3,4-Dihalo-2(5H )-furanones (X=Br, Cl) with Sulfoxides under Mild Conditions

Published:2017-08-16 Issue:17 Volume:359 Page:2961-2971
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Cao Liang¹,Luo Shi-He¹,Wu Han-Qing¹,Chen Liu-Qing¹,Jiang Kai¹,Hao Zhi-Feng²,Wang Zhao-Yang¹

Affiliation:

1. School of Chemistry and Environment; South China Normal University; Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education; Guangzhou 510006 People's Republic of China

2. School of Chemical Engineering and Light Industry; Guangdong University of Technology; Guangzhou 510006 People's Republic of China

Funder

Guangdong Natural Science Foundation

Guangdong Provincial Science and Technology Project

Guangzhou Science and Technology Project Scientific Special

Applied Science and Technology Research and Development Special Foundation of Guangdong Province

Publisher

Wiley

Subject

General Chemistry

Reference119 articles.

1. Recent advances in well-defined, late transition metal complexes that make and/or break C–N, C–O and C–S bonds

2. Cleavage of the C(O)–S Bond of Thioesters by Palladium/Norbornene/Copper Cooperative Catalysis: An Efficient Synthesis of 2-(Arylthio)aryl Ketones

3. Dysprosium(III)-Catalyzed Ring-Opening ofmeso-Epoxides: Desymmetrization by Remote Stereocontrol in a Thiolysis/Elimination Sequence

4. Dysprosium(III)-Catalyzed Ring-Opening ofmeso-Epoxides: Desymmetrization by Remote Stereocontrol in a Thiolysis/Elimination Sequence

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