SCHEDULED MAINTENANCE
The total synthesis of C-glycosyl angucycline, urdamycinone B 1, was achieved via C-glycosidation of naphthol 6 and the unprotected D-olivose 7, and Diels–Alder reaction of the unprotected C-glycosyl juglone 9 and the diene 17 as the key steps.
G. Matsuo, Y. Miki, M. Nakata, S. Matsumura and K. Toshima, Chem. Commun., 1996, 225 DOI: 10.1039/CC9960000225
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.
Please wait while we load your content...
