18O Assisted Analysis of a γ,δ-Epoxyketone Cyclization: Synthesis of the C16−C28 Fragment of Ammocidin D-Reference-Cited by-同舟云学术

18O Assisted Analysis of a γ,δ-Epoxyketone Cyclization: Synthesis of the C16−C28 Fragment of Ammocidin D

Published:2011-01-19 Issue:4 Volume:13 Page:756-759
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chau Stephen T.¹,Hayakawa Yoichi¹,Sulikowski Gary A.¹

Affiliation:

1. Departments of Chemistry and Biochemistry, Vanderbilt University, Vanderbilt Institute of Chemical Biology, Nashville, Tennessee 37235, United States, and Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol103003f

Reference24 articles.

1. Ammocidin, a New Apoptosis Inducer in Ras-dependent Cells from Saccharothrix sp. I. Production, Isolation and Biological Activity.

2. Ammocidin, a New Apoptosis Inducer in Ras-dependent Cells from Saccharothrix sp. II. Physico-chemical Properties and Structure Elucidation.

3. Ammocidins B, C and D, new cytotoxic 20-membered macrolides from Saccharothrix sp. AJ9571

4. Structure of Apoptolidin, a Specific Apoptosis Inducer in Transformed Cells

5. Water Overcomes Methyl Group Directing Effects in Epoxide-Opening Cascades

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