Catalytic Asymmetric Alkynylation of 3,4‐Dihydro‐β‐carbolinium Ions Enables Collective Total Syntheses of Indole Alkaloids-Reference-Cited by-同舟云学术

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Catalytic Asymmetric Alkynylation of 3,4‐Dihydro‐β‐carbolinium Ions Enables Collective Total Syntheses of Indole Alkaloids

Published:2021-10-20 Issue:47 Volume:133 Page:25339-25346
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Liang Lixin¹,Zhou Shiqiang¹,Zhang Wei¹,Tong Rongbiao¹²^ORCID

Affiliation:

1. Department of Chemistry The Hong Kong University of Science and Technology Clear Water Bay, Kowloon Hong Kong China

2. Hong Kong Branch of the Guangdong Southern Marine Science and Engineering Laboratory (Guangzhou) The Hong Kong University of Science and Technology Clear Water Bay, Kowloon Hong Kong China

Funder

Research Grants Council, University Grants Committee

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202112383

Reference141 articles.

2. The simple β-carboline alkaloids

3. Chemistry and biology of monoterpene indole alkaloid biosynthesis

4. Tetrahydro-β-carboline Alkaloids Occur in Fruits and Fruit Juices. Activity as Antioxidants and Radical Scavengers

5. The Discovery of Tadalafil: A Novel and Highly Selective PDE5 Inhibitor. 1: 5,6,11,11a-Tetrahydro-1H-imidazo[1‘,5‘:1,6]pyrido[3,4-b]indole-1,3(2H)-dione Analogues

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1. Total Syntheses of (+)‐Villocarine A, (−)‐Apogeissoschizine, and (+)‐Geissoschizine;Chemistry – A European Journal;2023-02-16

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