Facile Syntheses of (S,S)-2,3-Diaminobutyric Acid and the Acid Containing N-Terminal Tripeptide of Antrimycins.
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/21/1/21_1_49/_pdf
Reference8 articles.
1. Antrimycin, a new peptide antibiotic.
2. Isolation and structures of new peptide antibiotics, cirratiomycin A and B.
3. Facile synthesis of C-terminal .DELTA.2-dehydrotripeptides of antrimycins and cirratiomycins.
4. 4) Y. Nakamura and C. Shin, Chem. Lett., in press.
5. Lavendomycin, a new antibiotic. I. Taxonomy, isolation and characterization.
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2. Straightforward and Stereoselective Synthesis of α,β-Diamino Acid Derivatives by Means of an Organocatalyzed Decarboxylative Mannich Reaction;European Journal of Organic Chemistry;2017-06-08
3. Update 1 of: α,β-Diamino Acids: Biological Significance and Synthetic Approaches;Chemical Reviews;2011-02-09
4. ChemInform Abstract: Facile Syntheses of (S,S)-2,3-Diaminobutyric Acid and the Acid Containing N-Terminal Tripeptide of Antrimycins.;ChemInform;2010-08-21
5. A Novel Method for the Asymmetric Synthesis ofα,β-Diamino Acids by a Glucose-Mediated StereoselectiveStrecker Reaction;Helvetica Chimica Acta;2007-05
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