Synthesis of cyclopropa[c]indeno[1,2-b]quinolines through a MCR/Staudinger/aza-Wittig sequence-Reference-Cited by-同舟云学术

Synthesis of cyclopropa[c]indeno[1,2-b]quinolines through a MCR/Staudinger/aza-Wittig sequence

Published:2017-06-16 Issue:15 Volume:47 Page:1368-1374
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Nie Bing-Jie¹,Wu Li-Hui¹,Hu Ruo-Fei¹,Sun Yang¹,Wu Jing¹,He Ping¹^ORCID,Huang Nian-Yu²

Affiliation:

1. College of Chemical Engineering and Food Science, Hubei University of Arts and Science, Xiangyang, Hubei, China

2. Hubei Key Laboratory of Natural Products Research and Development, College of Biological and Pharmaceutical Sciences, China Three Gorges University, Yichang, Hubei, China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2017.1328065

Reference48 articles.

1. Multiple Multicomponent Macrocyclizations (MiBs): A Strategic Development Toward Macrocycle Diversity

2. Natural Product Synthesis Using Multicomponent Reaction Strategies

3. Palladium-Catalyzed Regioselective C–H Bond Acetoxylation–Alkoxylation of Azoxybenzenes

4. Multicomponent Coupling Reaction Using Arynes: Synthesis of Xanthene Derivatives

5. Multicomponent Reaction Design in the Quest for Molecular Complexity and Diversity

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