Asymmetric Total Synthesis of Indole Diterpenes Paspalicine, Paspalinine, and Paspalinine‐13‐ene-Reference-Cited by-同舟云学术

Asymmetric Total Synthesis of Indole Diterpenes Paspalicine, Paspalinine, and Paspalinine‐13‐ene

Published:2021-11-27 Issue:3 Volume:61 Page:
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angewandte Chemie Intl Edit

Author:

Guo Lian‐Dong¹,Xu Zejun¹,Tong Rongbiao¹²³^ORCID

Affiliation:

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

3. HKUST Shenzhen Research Institute Shenzhen 518057 China

Funder

National Natural Science Foundation of China

Research Grants Council, University Grants Committee

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202115384

Reference82 articles.

2. Tremorgenic Indole Alkaloids Potently Inhibit Smooth Muscle High-Conductance Calcium-Activated Potassium Channels

3. Terpendoles, Novel ACAT Inhibitors Produced by Albophoma yamanashiensis. I. Production, Isolation and Biological Properties.

4. TREMORGENIC AND NONTREMORGENIC 2,3-FUSED INDOLE DITERPENOIDS

5. A Novel Indole-diterpenoid, JBIR-03 with Anti-MRSA Activity from Dichotomomyces cejpii var. cejpii NBRC 103559

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