Syntheses of the tedanolides
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2008/NP/B719607E
Reference48 articles.
1. Tedanolide: a potent cytotoxic macrolide from the Caribbean sponge Tedania ignis
2. Bioactive marine metabolites. Part 35. Cytotoxic metabolites of the marine sponge Mycale adhaerens Lambe
3. 13-Deoxytedanolide, a marine sponge-derived antitumor macrolide, binds to the 60S large ribosomal subunit
4. Structure–activity relationship study on 13-deoxytedanolide, a highly antitumor macrolide from the marine sponge Mycale adhaerens
5. The Structures of Antibiotics Bound to the E Site Region of the 50 S Ribosomal Subunit of Haloarcula marismortui: 13-Deoxytedanolide and Girodazole
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1. Development of the Synthesis of Desepoxy-Tedanolide C;The Journal of Organic Chemistry;2024-01-25
2. Synthesis of Desepoxy‐Tedanolide C;Chemistry – A European Journal;2021-04-09
3. Studies towards the synthesis of tedanolide C. Construction of the C13-epi C1–C15 fragment;Organic & Biomolecular Chemistry;2016
4. Porifera (Sponges)-5;Encyclopedia of Marine Natural Products;2014-08-07
5. Directed studies towards the total synthesis of (+)-13-deoxytedanolide: simple and convenient synthesis of the C8–C16 fragment;Organic & Biomolecular Chemistry;2013
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