Asymmetric Total Syntheses of the Akuammiline Alkaloids (−)‐Strictamine and (−)‐Rhazinoline-Reference-Cited by-同舟云学术

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Asymmetric Total Syntheses of the Akuammiline Alkaloids (−)‐Strictamine and (−)‐Rhazinoline

Published:2019-04-23 Issue:18 Volume:58 Page:6059-6063
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Li Wenfei¹,Chen Zhitao²,Yu Di¹,Peng Xin¹,Wen Guohua¹,Wang Siqi¹,Xue Fei¹,Liu Xiao‐Yu¹^ORCID,Qin Yong¹^ORCID

Affiliation:

1. Key Laboratory of Drug-Targeting and Drug Delivery System of the Education MinistrySichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial TechnologyWest China School of PharmacySichuan University Chengdu 610041 P. R. China

2. School of Pharmaceutic ScienceChongqing University Chongqing 401331 P. R. China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201901074

Reference96 articles.

1. For selected reviews of akuammiline alkaloids see:

2. Current Progress in the Chemistry and Pharmacology of Akuammiline Alkaloids

3. The Akuammiline Alkaloids; Origin and Synthesis

4. Cascade Reactions: A Driving Force in Akuammiline Alkaloid Total Synthesis

5. Kaskadenreaktionen in der Totalsynthese von Akuammilin-Alkaloiden

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1. Terminating E-ring cyclizations for caged indole alkaloids: The secret to success?;Tetrahedron Letters;2024-10

2. Construction of the Akuammiline Alkaloid Core Structure via Stereoselective E-Ring Formation;The Journal of Organic Chemistry;2024-07-02

3. Enantioselective Aminative Dearomatization of Indoles via Electrophilic 1,6-Addition of p-Quinone Diimides (p-QDIs);Organic Letters;2024-06-03

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