Assembly of the Isoindolinone Core of Muironolide A by Asymmetric Intramolecular Diels–Alder Cycloaddition-Reference-Cited by-同舟云学术

Assembly of the Isoindolinone Core of Muironolide A by Asymmetric Intramolecular Diels–Alder Cycloaddition

Published:2011-07-13 Issue:15 Volume:13 Page:3932-3935
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Flores Beatris¹,Molinski Tadeusz F.¹

Affiliation:

1. Department of Chemistry and Biochemistry and Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, 9500 Gilman Drive MC0358, La Jolla, California 92093, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol201461n

Reference26 articles.

1. Peloruside A: A Potent Cytotoxic Macrolide Isolated from the New Zealand Marine Sponge Mycale sp.

2. Halichondrin B and homohalichondrin B, marine natural products binding in the vinca domain of tubulin. Discovery of tubulin-based mechanism of action by analysis of differential cytotoxicity data

3. A Tetrachloro Polyketide Hexahydro-1H-isoindolone, Muironolide A, from the Marine Sponge Phorbas sp. Natural Products at the Nanomole Scale

4. Phorboxazoles A and B: potent cytostatic macrolides from marine sponge Phorbas species

5. Absolute Configuration of Phorboxazoles A and B from the Marine Sponge Phorbas sp. 1. Macrolide and Hemiketal Rings

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