Convenient Synthesis of Dehydrooligopeptides Containing α-Dehydroamino Acid Residue Alone
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/23/10/23_10_1909/_pdf
Reference6 articles.
1. The structures of A10255 B, -G and -J: new thiopeptide antibiotics produced by Streptomyces gardneri
2. Ca2+ binding cyclic octapeptides having an alternating sar and a hydrophobic amino acid in the sequence
3. Dehydrooligopeptides. XIV. Convenient Coupling ofN-Carboxy-α-dehydroamino Acid Anhydride with Both Amine and Carboxyl Components
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. ChemInform Abstract: Convenient Synthesis of Dehydrooligopeptides Containing α- Dehydroamino Acid Residue Alone.;ChemInform;2010-08-18
2. Novel Synthesis of the Main Central 2,3,6-Trisubstituted Pyridine Skeleton [Fragment A-B-C] of a Macrobicyclic Antibiotic, Cyclothiazomycin;Bulletin of the Chemical Society of Japan;2002-07
3. Dehydrooligopeptides. XIV. Syntheses of 2-[(Z)-1-Amino-1-alken-1-yl]oxazole-4-carboxylic Acid and the Main Common Skeleton of Thiostrepton Peptide Antibiotics, A10255G and J;Bulletin of the Chemical Society of Japan;1996-08
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