Synthese des all-L-Konfigurierten CyclotetradepsipeptidsCyclo[-L-Val-L-Lac-]2 nach dem kombinierten Schutz-/ Aktivierungsverfahren mit der 2,4-Bis(methylthio)phenoxycarbonyl-Gruppe
Author:
Publisher
Wiley
Subject
General Medicine
Reference10 articles.
1. Biosynthesis of actinomycin D : Purification and properties of an enzyme which activates L-valine
2. On the origin ofd-aminoacid residues in microbial peptides
3. Synthese des all-L-konfigurierten Cyclohexadepsipeptidscyclo-[L-Val-L-Lac]3 nach der Peoc/Säurechlorid-Methode
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1. Triblock Peptide and Peptide Thioester Synthesis With Reactivity-Differentiated Sulfonamides and Peptidyl Thioacids;Angewandte Chemie International Edition;2009-09-28
2. Triblock Peptide and Peptide Thioester Synthesis With Reactivity-Differentiated Sulfonamides and Peptidyl Thioacids;Angewandte Chemie;2009-09-28
3. Survey of conformational role of ester bonds in a cyclic depsipeptide;International Journal of Peptide and Protein Research;2009-01-12
4. Through-bond modulation of reaction centers by remote substituents;Small Ring Compounds in Organic Synthesis IV;1990
5. ChemInform Abstract: Synthesis of the all-L-Configurated Cyclotetradepsipeptide cyclo[-L-Val-L-Lac-]2by the Combined Protection/Activation Method with the 2,4-Bis(methylthio)phenoxycarbonyl Group.;Chemischer Informationsdienst;1986-06-03
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