Abstract
The most extensive single project in the history of organic chemistry—the total synthesis of erythromycin A and B—has received new impetus from biosynthetic studies (see related Highlight in the last edition) as well as from a new approach for the final steps of the chemical synthesis. The sequence of first lactonization, then glycosidation has been assumed incontestable; however, the reversed order of reactions recently led to considerable success. The story continues…
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 callMore From: Angewandte Chemie International Edition in English
Disclaimer: 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.
