Abstract
AbstractCapuramycin is an important lead nucleoside antibiotic for the development of new therapeutic agents against the multidrug‐resistant Mycobacterium tuberculosis infections. Due to the poor accessibilities, the heterogeneous issues and difficulties in the modification of capuramycin at the specific positions, in‐depth studies on the structure‐activity relationships (SAR) of capuramycin are hampered. Chemical synthesis is a reliable and effective method to provide capuramycin and its analogues. Thus far, only four different synthetic routes toward capuramycin have been reported. Herein, we provide a comprehensive review on the chemical synthesis of capuramycin.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
