Stereocontrolled Total Synthesis of (−)-Eudistomin C
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja055832h
Reference30 articles.
1. Eudistomins C, E, K, and L, potent antiviral compounds containing a novel oxathiazepine ring from the Caribbean tunicate Eudistoma olivaceum
2. Eudistomins A, D, G, H, I, J, M, N, O, P, and Q, bromo, hydroxy, pyrrolyl and iminoazepino .beta.-carbolines from the antiviral Caribbean tunicate Eudistoma olivaceum
3. Eudistomins A-Q, .beta.-carbolines from the antiviral Caribbean tunicate Eudistoma olivaceum
4. Eudistomidin-A, a novel calmodulin antagonist from the okinawan tunicate
5. Eudistomin K sulfoxide - an antiviral sulfoxide from the New Zealand ascidian Ritterella sigillinoides
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