Zinc-Catalyzed Tandem Diels-Alder Reactions of Enynals with Alkenes: Generation and Trapping of Cyclico-Quinodimethanes (o-QDMs)-Reference-Cited by-同舟云学术

Zinc-Catalyzed Tandem Diels-Alder Reactions of Enynals with Alkenes: Generation and Trapping of Cyclico-Quinodimethanes (o-QDMs)

Published:2016-06-15 Issue:16 Volume:358 Page:2684-2691
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Zhang Jiantao¹,Xiao Yelin¹,Chen Kai¹,Wu Wanqing¹,Jiang Huanfeng¹,Zhu Shifa¹

Affiliation:

1. Key Laboratory 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

Funder

National Natural Science Foundation of China

Guangdong Natural Science Foundation

China Postdoctoral Science Foundation

SRF for ROCS

State Education Ministry

Fundamental Research Funds for the Central Universities, SCUT

Publisher

Wiley

Subject

General Chemistry

Reference44 articles.

1. AuCl3-Catalyzed Benzannulation: Synthesis of Naphthyl Ketone Derivatives from o-Alkynylbenzaldehydes with Alkynes

2. Functionalized 1,2-Dihydronaphthalenes from the Cu(OTf)2-Catalyzed [4+2] Cycloaddition of o-Alkynyl(oxo)benzenes with Alkenes

3. Lewis Acid-Catalyzed Benzannulation via Unprecedented [4+2] Cycloaddition of o-Alkynyl(oxo)benzenes and Enynals with Alkynes

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