Diastereoselective pictet-spengler reactions of L-(boc)prolinal: a biomimetic synthesis of eudistomins H and I, and woodinine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 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. Three new β-carbolines from the bermudian tunicate Eudistoma olivaceum
5. Eudistomidin-A, a novel calmodulin antagonist from the okinawan tunicate
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3. Ascidians (Tunicates)-2;Encyclopedia of Marine Natural Products;2014-08-07
4. Diastereoselective Pictet–Spengler Reactions of a Tethered 2-Aminoimidazole;Australian Journal of Chemistry;2014
5. Synthesis of Bioactive 2-Aza-Analogues of Ipecac and Alangium Alkaloids;ChemMedChem;2010-06-23
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