Synthetic Studies on Quinoxaline Antibiotics. Synthesis of Quinoxaline-2-carbonyl Tetradepsipeptide Derivatives Related to Triostin A
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/51/5/51_5_1501/_pdf
Reference35 articles.
1. Configuration of N,β-Dimethylleucine, a Constituent Amino Acid of Triostin C
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1. Syntheses of Triostin A Antibiotic and Nucleobase-Functionalized Analogs as New DNA Binders;European Journal of Organic Chemistry;2009-10
2. Probing Host-Selective Phytotoxicity: Synthesis of Destruxin B and Several Natural Analogues;The Journal of Organic Chemistry;2001-10-17
3. Synthesis of a model analog of the cyclic decadepsipeptide intercalating agent luzopeptin A (antibiotic BBM 928A) containing proline, valine, and unsubstituted quinoline substituents;The Journal of Organic Chemistry;1986-08
4. Bis(2-oxo-3-oxazolidinyl)phosphinic chloride (1) as a coupling reagent for N-alkyl amino acids;Journal of the American Chemical Society;1985-07
5. Synthetic Studies on Quinoxaline Antibiotics. II. Synthesis of Triostin A;Bulletin of the Chemical Society of Japan;1984-08
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