Short Formal Syntheses of Lycorine and Congeners Using a 5<i>-Endo-Trig</i>/6<i>-Endo-Trig</i> Radical Cyclization Sequence-Reference-Cited by-同舟云学术

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Short Formal Syntheses of Lycorine and Congeners Using a 5-Endo-Trig/6-Endo-Trig Radical Cyclization Sequence

Published:2024-05-10 Issue:20 Volume:26 Page:4292-4296
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Tan Shen¹²,Zard Samir Z.²^ORCID,Pham Le Nhan³^ORCID,Coote Michelle L.³^ORCID,Banwell Martin G.¹,Lan Ping¹^ORCID,White Lorenzo V.¹²^ORCID

Affiliation:

1. Institute for Advanced and Applied Chemical Synthesis, College of Pharmacy, Jinan University, Guangzhou, Guangdong 510632, China

2. Laboratoire de Synthèse Organique, CNRS, École Polytechnique, Palaiseau 91128, France

3. Institute for Nanoscale Science and Technology, College of Science and Engineering, Flinders University, Adelaide, South Australia 5042, Australia

Funder

Ministry of Science and Technology of the People's Republic of China

Australian Research Council

National Natural Science Foundation of China

Guangdong Science and Technology Plan International Collaboration Topic

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01271

Reference27 articles.

1. Developing therapeutic approaches for twenty-first-century emerging infectious viral diseases

2. The Inhibition of RNA Viruses by Amaryllidaceae Alkaloids: Opportunities for the Development of Broad‐Spectrum Anti‐Coronavirus Drugs

3. Lycorine: A prospective natural lead for anticancer drug discovery

4. Total synthesis of the amaryllidaceae alkaloids, lycorine and zephyranthine

5. Short, enantioselective, gram-scale synthesis of (−)-zephyranthine

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