Total Solid-Phase Synthesis of Dehydroxy Fengycin Derivatives
Author:
Affiliation:
1. LIPPSO, Department of Chemistry, University of Girona, Maria Aurèlia Capmany 69, 17003 Girona, Spain
Funder
European Regional Development Fund
Ministerio de Econom?a y Competitividad
Universitat de Girona
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b02553
Reference46 articles.
1. Bacillus subtilis antibiotics: structures, syntheses and specific functions
2. Bacillus lipopeptides: versatile weapons for plant disease biocontrol
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4. Cyclic Lipodepsipeptides in Novel Antimicrobial Drug Discovery
5. Learning from Nature's Drug Factories: Nonribosomal Synthesisof MacrocyclicPeptides
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1. Increasing fengycin production by strengthening the fatty acid synthesis pathway and optimizing fermentation conditions;Biochemical Engineering Journal;2022-01
2. Research Progress of Fengycin Biosynthesis;Advances in Analytical Chemistry;2022
3. Fengycin A Analogues with Enhanced Chemical Stability and Antifungal Properties;Organic Letters;2021-06-02
4. Solid-Phase Synthesis of Head to Side-Chain Tyr-Cyclodepsipeptides Through a Cyclative Cleavage From Fmoc-MeDbz/MeNbz-resins;Frontiers in Chemistry;2020-04-22
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