Asymmetric Inverse-Electron-Demand Diels–Alder Reaction of β,γ-Unsaturated Amides through Dienolate Catalysis-Reference-Cited by-同舟云学术

Asymmetric Inverse-Electron-Demand Diels–Alder Reaction of β,γ-Unsaturated Amides through Dienolate Catalysis

Published:2019-08-29 Issue:18 Volume:21 Page:7337-7341
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Qin Jialiang¹,Zhang Yili¹,Liu Cuiting²,Zhou Jun³,Zhan Ruoting¹,Chen Weiwen¹,Huang Huicai¹^ORCID

Affiliation:

1. Research Center of Chinese Herbal Resource Science and Engineering, Key Laboratory of Chinese Medicinal Resource from Lingnan, Ministry of Education, Guangzhou University of Chinese Medicine, Guangzhou 510006, China

2. Central Laboratory, Southern Medical University, Guangzhou 510515, China

3. School of Chemistry and Food Engineering, Changsha University of Science and Technology, Changsha 410114, China

Funder

Guangzhou University of Chinese Medicine

Department of Education of Guangdong Province

Pearl River Talents Recruitment Program of Guangdong Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02629

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3. Syntheses of (−)-Oleocanthal, a Natural NSAID Found in Extra Virgin Olive Oil, the (−)-Deacetoxy-Oleuropein Aglycone, and Related Analogues

4. Synthesis of Xyloketals, Natural Products from the Mangrove FungusXylaria sp

5. Isolation, biological activity, synthesis, and medicinal chemistry of the pederin/mycalamide family of natural products

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