Characterization of a new component and impurities in josamycin by trap‐free two‐dimensional liquid chromatography coupled to ion trap time‐of‐flight mass spectrometry
Author:
Affiliation:
1. Zhejiang University of Technology Hangzhou 310014 China
2. Zhejiang Institute for Food and Drug Control Hangzhou 310052 China
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Analytical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/rcm.8439
Reference28 articles.
1. Modifications and Biological Activity of Natural and Semisynthetic 16-Membered Macrolide Antibiotics
2. Conversion of leucomycin-A3 antibiotic into novel triazole analogues via regio- and diastereoselective SN1′ substitution with allylic rearrangement and 1,3-dipolar cycloaddition of CuAAC type
3. Structure elucidation, complete NMR assignment and PM5 theoretical studies of new hydroxy-aminoalkyl-α,β-unsaturated derivatives of the macrolide antibiotic josamycin
4. Synthesis and antibacterial activity of a series of novel 9-O-acetyl- 4′-substituted 16-membered macrolides derived from josamycin
5. Unexpected α,β-unsaturated products of reductive amination of the macrolide antibiotic josamycin
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