ArticleOrganic letters2012
Toward an enantioselective synthesis of (-)-zampanolide: preparation of the C9-C20 region.
Article in Organic letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
7 citing papers in PubMed.
- Article
- Article
- Total Synthesis and Structural Reassignment of Lyngbyaloside C Highlighted by Intermolecular Ketene Esterification.Chemistry (Weinheim an der Bergstrasse, Germany) · 2015Article
- Zampanolide and dactylolide: cytotoxic tubulin-assembly agents and promising anticancer leads.Natural product reports · 2014Review
- Conformational preferences of zampanolide and dactylolide.Organic letters · 2013Article
- Concise enantioselective synthesis of diospongins A and B.Tetrahedron · 2013Article
- Macrocyclic drugs and synthetic methodologies toward macrocycles.Molecules (Basel, Switzerland) · 2013Review
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Progress toward the synthesis of the microtubule-stabilizing agent, (-)-zampanolide, is reported. Construction of the 2,6-cis-tetrahydropyran ring was accomplished utilizing ether transfer methodology in conjunction with an intramolecular radical cyclization reaction. Efficient installation of the C16-C20 side chain relied on a one-pot cross-metathesis/olefination sequence, Sharpless epoxidation, and selective reduction of a vinyl epoxide.
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Registered trials
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