Stereocontrolled Total Synthesis of Muraymycin D1 Having a Dual Mode of Action against Mycobacterium tuberculosis
Author:
Affiliation:
1. Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, Tennessee 38163, United States
Funder
National Institute of Allergy and Infectious Diseases
University of Tennessee
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.6b07395
Reference51 articles.
1. Structures of the Muraymycins, Novel Peptidoglycan Biosynthesis Inhibitors
2. FTMS Structure Elucidation of Natural Products: Application to Muraymycin Antibiotics Using ESI Multi-CHEF SORI-CID FTMSn, the Top-Down/Bottom-Up Approach, and HPLC ESI Capillary-Skimmer CID FTMS
3. Muraymycin nucleoside-peptide antibiotics: uridine-derived natural products as lead structures for the development of novel antibacterial agents
4. Antimicrobial nucleoside antibiotics targeting cell wall assembly: Recent advances in structure–function studies and nucleoside biosynthesis
5. Recent advances in antimicrobial nucleoside antibiotics targeting cell wall biosynthesis
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