Asymmetric Total Synthesis of Brasilicardins-Reference-Cited by-同舟云学术

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Asymmetric Total Synthesis of Brasilicardins

Published:2018-11-28 Issue:52 Volume:57 Page:17161-17167
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Yoshimura Fumihiko¹²^ORCID,Itoh Ryusei³,Torizuka Makoto³,Mori Genki¹,Tanino Keiji¹^ORCID

Affiliation:

1. Department of Chemistry Faculty of Science Hokkaido University Sapporo 060-0810 Japan

2. Present address: School of Pharmaceutical Sciences University of Shizuoka 52-1 Yada Suruga-ku Shizuoka 422-8526 Japan

3. Graduate School of Chemical Sciences and Engineering Hokkaido University Sapporo 060-0810 Japan

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201811403

Reference32 articles.

1. Brasilicardin A. A Novel Tricyclic Metabolite with Potent Immunosuppressive Activity from Actinomycete Nocardia brasiliensis

2. Brasilicardins B–D, new tricyclic terpernoids from actinomycete Nocardia brasiliensis

3. Brasilicardin A, a New Terpenoid Antibiotic from Pathogenic Nocardia brasiliensis: Fermentation, Isolation and Biological Activity.

4. Brasilicardin A, a Natural Immunosuppressant, Targets Amino Acid Transport System L

5. SAR studies of brasilicardin A for immunosuppressive and cytotoxic activities

Cited by 17 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. Multiple regulators control the biosynthesis of brasilicardin inNocardia terpenica;2024-06-11

2. Gold-catalyzed cyclization and cycloaddition in natural product synthesis;Natural Product Reports;2024

3. A Journey to the Total Synthesis of Brasilicardins;Modern Natural Product Synthesis;2024

4. Synthesis of a Complex Brasilicardin Analogue Utilizing a Cobalt-Catalyzed MHAT-Induced Radical Bicyclization Reaction;Organic Letters;2023-05-04

5. Beyond classical sulfone chemistry: metal- and photocatalytic approaches for C–S bond functionalization of sulfones;Chemical Society Reviews;2022

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