Synthesis of the South hexacyclic sterold unit of cephalostatin 7
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Antineoplastic agents 285. Isolation and structures of cephalostatins 14 and 15
2. Ritterazine A, a highly cytotoxic dimeric steroidal alkaloid, from the tunicate Ritterella tokioka
3. Antineoplastic agents. 214. Isolation and structure of cephalostatins 7-9
4. Synthesis of a 17-Deoxy, C-14,15-Dihydro Derivative of the North Spiroketal Moiety of the Cephalostatins. Conversion to a (+)-Trisdecacyclic C2 Symmetrical Pyrazine
5. Spiroketal equilibration: Interconversion of 1,6-dioxaspiro[4.4]nonanes and 1,6-dioxaspiro[4.5]decanes. Implications for the synthesis of cephalostatin 7
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1. Wormlike Organisms: 2. Chaetognatha and Hemichordata (Enteropneusta and Pterobranchia);Encyclopedia of Marine Natural Products;2014-08-07
2. Cephalostatins and Ritterazines;The Alkaloids: Chemistry and Biology;2013
3. Biomimetic Syntheses of Alkaloids with a Non-Amino Acid Origin;Biomimetic Organic Synthesis;2011-04-21
4. Chemistry of Trisdecacyclic Pyrazine Antineoplastics: The Cephalostatins and Ritterazines † This review is dedicated to the community of isolation/identification natural product detectives, with special thanks to the groups of Bob Pettit and Nobuhiro Fusatani.;Chemical Reviews;2009-05-13
5. Catalytic Epoxidation and syn-Dihydroxylation Reactions in Steroid Chemistry;Current Organic Chemistry;2008-04-01
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