Studies toward the Synthesis of an Oxazole-Based Analog of (−)-Zampanolide-Reference-Cited by-同舟云学术

Studies toward the Synthesis of an Oxazole-Based Analog of (−)-Zampanolide

Published:2021-02-26 Issue:6 Volume:23 Page:2238-2242
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Bold Christian P.¹,Klaus Cindy¹^ORCID,Pfeiffer Bernhard¹,Schürmann Jasmine¹,Lombardi Rafael¹,Lucena-Agell Daniel²,Díaz J. Fernando²^ORCID,Altmann Karl-Heinz¹^ORCID

Affiliation:

1. ETH Zürich, Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, Vladimir-Prelog-Weg 4, 8093 Zürich, Switzerland

2. Centro de Investigaciones Biológicas Margarita Salas, Consejo Superior de Investigaciones Científicas, Ramiro de Maeztu 9, 28040 Madrid, Spain

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Ministerio de Ciencia e Innovación

H2020 Marie Sklodowska-Curie Actions

Fondo de Investigaciones Sanitarias

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c00378

Reference35 articles.

1. Zampanolide, a new cytotoxic marcrolide from a marine sponge

2. Microtubule-Stabilizing Activity of Zampanolide, a Potent Macrolide Isolated from the Tongan Marine Sponge Cacospongia mycofijiensis

3. Recent advances in microtubule-stabilizing agents

4. Molecular Mechanism of Action of Microtubule-Stabilizing Anticancer Agents

5. Macrolactonization via Ti(IV)-Mediated Epoxy-Acid Coupling: A Total Synthesis of (−)-Dactylolide [and Zampanolide]

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