Enantioselective total synthesis of callipeltoside A: two approaches to the macrolactone fragment-Reference-Cited by-同舟云学术

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Enantioselective total synthesis of callipeltoside A: two approaches to the macrolactone fragment

Published:2008-05 Issue:21 Volume:64 Page:4671-4699
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Evans David A.,Burch Jason D.,Hu Essa,Jaeschke Georg

Funder

National Institutes of Health

Merck

National Science Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference79 articles.

1. Callipeltoside A: A Cytotoxic Aminodeoxy Sugar-Containing Macrolide of a New Type from the Marine Lithistida Sponge Callipelta sp.

2. Callipeltosides B and C, two novel cytotoxic glycoside macrolides from a marine lithistida sponge Callipelta sp.

3. Total Syntheses:

4. Callipeltoside A: Assignment of Absolute and Relative Configuration by Total Synthesis We thank the National Science Foundation and the National Institutes of Health for their generous support of our programs. OD was supported in part by a fellowship from the Association pour la Recherche contre le Cancer (ARC). J.L.G. was supported in part by a NIH postdoctoral fellowship from the National Cancer Institute. Mass spectra were provided by the Mass Spectroscopy Facility at the University of California, San Francisco supported by the NIH Division of Research Resources, and the Mass Spectrometry Facility at University of California, Irvine. We thank Dr. John Greaves of the latter facility for his assistance.

5. Enantioselective Total Synthesis of Callipeltoside A

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