Asymmetric Total Synthesis of Aglacins A, B, and E-Reference-Cited by-同舟云学术

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Asymmetric Total Synthesis of Aglacins A, B, and E

Published:2021-06-22 Issue:30 Volume:133 Page:16791-16796
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Xu Mengmeng¹,Hou Min¹,He Haibing²,Gao Shuanhu¹²^ORCID

Affiliation:

1. Shanghai Key Laboratory of Green Chemistry and Chemical, Processes School of Chemistry and Molecular Engineering East China Normal University China

2. Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development East China Normal University 3663 North Zhongshan Road Shanghai 200062 China

Funder

National Natural Science Foundation of China

Program of Shanghai Academic Research Leader

Fundamental Research Funds for Central Universities of the Central South University

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202105395

Reference92 articles.

1. Pharmakologische Studien über Podophyllum peltatum

2. For selective review articles on aryltetralin lactone lignans see:

3. Advances in the Synthesis of Aryltetralin Lignan Lactones

4. The chemical synthesis of aryltetralin glycosides

5. Recent Advances in the Chemistry and Biology of Podophyllotoxins

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Late‐Stage Functionalization for the Divergent Synthesis of Podophyllotoxin Derivatives by Rhodium Catalysis;Chemistry – A European Journal;2023-05-26

2. Asymmetric Total Synthesis of Hasubanan Alkaloids: Periglaucines A–C, N,O ‐Dimethyloxostephine and Oxostephabenine;Angewandte Chemie International Edition;2022-12-02

3. Asymmetric Total Synthesis of Hasubanan Alkaloids: Periglaucines A–C, N,O ‐Dimethyloxostephine and Oxostephabenine;Angewandte Chemie;2022-12-02

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