Synthesis of a Common Main Skeleton of Thiostrepton Peptide Antibiotics, A10255G and J
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/23/7/23_7_1305/_pdf
Reference5 articles.
1. The structures of A10255 B, -G and -J: new thiopeptide antibiotics produced by Streptomyces gardneri
2. Facile and useful one-pot synthesis of dehydrooligopeptides using ΔNCA
3. Formation of oxazolines and thiazolines in peptides by the mitsunobu reaction
Cited by 5 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: Synthesis of a Common Main Skeleton of Thiostrepton Peptide Antibiotics, A 10255G and J.;ChemInform;2010-08-18
2. Stereoselective Syntheses of (E)-α,β-Dehydroamino Acids and (E)-α,β-Dehydropeptides by Stereospecific Dehydration with 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC);Synthesis;2003
3. Diastereoselective Aldol Reactions of (Z)-N-[Bis(methylthio)methylene]-α,β-didehydroglutamates;The Journal of Organic Chemistry;1998-11-01
4. 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
5. A new and efficient preparation of α,β-dehydroamino acids;Tetrahedron Letters;1995-05
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