Base-Promoted Addition of Arylacetonitriles to Terminal Alkynes: Regio- and Stereoselective Access to Disubstituted Acrylonitriles-Reference-Cited by-同舟云学术

Base-Promoted Addition of Arylacetonitriles to Terminal Alkynes: Regio- and Stereoselective Access to Disubstituted Acrylonitriles

Published:2017-02-21 Issue:8 Volume:359 Page:1339-1350
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Qi Chaorong¹²,Peng Youbin²,Ouyang Lu²,Ren Yanwei²,Jiang Huanfeng²

Affiliation:

1. School of Chemistry and Chemical Engineering, State Key Lab of Luminescent Materials and Devices; South China University of Technology; Guangzhou 510640 People's Republic of China

2. Key Lab of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering; South China University of Technology; Guangzhou 510640 People's Republic of China, Fax: (+86)-20-8711-2906

Funder

National Program on Key Research Project

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

General Chemistry

Reference114 articles.

1. Nitrile-containing natural products

2. Nitrile-Containing Pharmaceuticals: Efficacious Roles of the Nitrile Pharmacophore

3. Designer Magnets Containing Cyanides and Nitriles

4. Synthesis and evaluation of a series of benzothiophene acrylonitrile analogs as anticancer agents

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