Efficient method for introducing vineomycin-fridamycin-type side chain. Total synthesis of fridamycin E
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. New antitumor antibiotics, OS-4742 A1, A2, B1 and B2 produced by a strain of Streptomyces.
2. The structure of vineomycin B2.
3. New approach to C-aryl glycosides starting from phenol and glycosyl fluoride. Lewis acid-catalyzed rearrangement of O-glycoside to C-glycoside
4. Synthetic study toward vineomycins. Synthesis of c-aryl glycoside sector via Cp2HfCl2AgClO4-promoted tactics
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3. Convergent de novo synthesis of vineomycinone B2 methyl ester;Chemical Communications;2013
4. De Novo Asymmetric Synthesis of Fridamycin E;Organic Letters;2011-11-22
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