Pd-Catalyzed sequential β-C(sp3)–H arylation and intramolecular amination of δ-C(sp2)–H bonds for synthesis of quinolinones via an N,O-bidentate directing group-Reference-Cited by-同舟云学术

Pd-Catalyzed sequential β-C(sp3)–H arylation and intramolecular amination of δ-C(sp2)–H bonds for synthesis of quinolinones via an N,O-bidentate directing group

Published:2016 Issue:43 Volume:52 Page:7043-7046
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Guan Mingyu¹²³⁴⁵,Pang Yubo¹²³⁴⁵,Zhang Jingyu¹²³⁴⁵,Zhao Yingsheng⁶⁷⁸⁹⁵

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province

2. College of Chemistry

3. Chemical Engineering and Materials Science Soochow University

4. Suzhou 215123

5. China

6. College of Physics

7. Optoelectronics and Energy & Collaborative Innovation Center of Suzhou Nano Science and Technology

8. Soochow University

9. Suzhou 215006

Abstract

An effective protocol for the synthesis of quinolinone derivatives by palladium-catalyzed sequential β-C(sp³)–H arylation and selective intramolecular C(sp²)–H/N–H amination is developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/CC/C6CC02865A

Reference47 articles.

1. The structural use of carbostyril in physiologically active substances

2. TTD: Therapeutic Target Database

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5. Continuing efforts on the improvement of Beckmann rearrangement of indanone oxime

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