Efficient construction of 3-arylquinolin-4(1 H )-ones via in situ Meinwald rearrangement/intramolecular reductive cyclization of 2′-nitrochalcone epoxides-Reference-Cited by-同舟云学术

Efficient construction of 3-arylquinolin-4(1 H )-ones via in situ Meinwald rearrangement/intramolecular reductive cyclization of 2′-nitrochalcone epoxides

Published:2016-11 Issue:44 Volume:72 Page:7025-7031
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Wang Sheng,Zhao Chao,Liu Ting,Yu Lifang,Yang Fan,Tang Jie

Funder

The National Key Technology R&D Program

Shanghai Science and Technology Council

Laboratory of Organic Functional Molecules

Sino-French Institute of ECNU

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference31 articles.

1. Palladium-Catalyzed Dehydrogenation/Oxidative Cross-Coupling Sequence of β-Heteroatom-Substituted Ketones

2. Pd-Catalyzed Dehydrogenative Cross-Coupling of Polyfluoroarenes with Heteroatom-Substituted Enones

3. Palladium-Catalyzed Oxidative Carbonylation for the Synthesis of Polycyclic Aromatic Hydrocarbons (PAHs)

4. Transition-Metal-Free C-3 Arylation of Quinoline-4-ones with Arylhydrazines

5. Discovery, Synthesis, and Optimization of Antimalarial 4(1H)-Quinolone-3-Diarylethers

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