Asymmetric total synthesis of (+)-tubingensin A-Reference-Cited by-同舟云学术

Asymmetric total synthesis of (+)-tubingensin A

Published:2023 Issue:1 Volume:10 Page:189-192
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zhai Hongbin¹²³⁴^ORCID,Liu Dong¹,Wang Taimin³

Affiliation:

1. The State Key Laboratory of Chemical Oncogenomics, Guangdong Provincial Key Laboratory of Nano-Micro Materials Research, School of Chemical Biology and Biotechnology, Shenzhen Graduate School of Peking University, Shenzhen 518055, China

2. Shenzhen Bay Laboratory, Shenzhen 518055, China

3. Institute of Marine Biomedicine, Shenzhen Polytechnic, Shenzhen 518055, China

4. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071, China

Abstract

A nine-step asymmetric total synthesis of (+)-tubingensin A has been realized.

Funder

Science, Technology and Innovation Commission of Shenzhen Municipality

Shenzhen Bay Laboratory

Science and Technology Planning Project of Guangdong Province

Shenzhen-Hong Kong Institute of Brain Science

National Ten Thousand Talent Program

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D2QO01540D

Reference29 articles.

1. Nominine: a new insecticidal indole diterpene from the sclerotia of Aspergillus nomius

2. Tubingensin A: an antiviral carbazole alkaloid from the sclerotia of Aspergillus tubingensis

3. Antiinsectan natural products from fungal sclerotia

4. Occurrence, Biogenesis, and Synthesis of Biologically Active Carbazole Alkaloids

5. Isolation and Synthesis of Biologically Active Carbazole Alkaloids

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