A Claisen rearrangement route to the vineomycins
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference3 articles.
1. Total synthesis of vineomycinone B2 methyl ester
2. Experiments directed towards the synthesis of anthracyclinones. VIII. Functionalization of hydroxyanthraquinones by reductive Claisen rearrangements
3. Experiments directed towards the synthesis of anthracyclinones. V. Double Claisen rearrangement of 1,4-Bis(allyloxy)anthraquinones
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1. The Total Synthesis of Naturally Occurring Quinones;Total Synthesis of Natural Products;2007-02-20
2. Synthesis of Anthraquinone Derivatives: Tandem Diels-Alder-Decarboxylation-Oxidation Reaction of 3-Hydroxy-2-pyrone with 1,4-Naphthoquinone;Synlett;2006
3. Synthesis of angularly-fused aromatic antibiotics. Preparation of the ABC ring system of aquayamycin;Tetrahedron Letters;1997-09
4. Titanium mediation of aldol reactions in fridamycin and vineomycinone syntheses;Tetrahedron Letters;1994-05
5. Total synthesis of vineomycinone B2 methyl ester via double Bradsher cyclization;Journal of the American Chemical Society;1991-07
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