| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5217362 | Tetrahedron | 2013 | 6 Pages |
Abstract
A compact synthesis of Murrayaquinone A is reported, based on sequential Buchwald-Hartwig amination/annulative C-H activation followed by oxidation of the intermediate carbazole. The methodology can be readily extended to other analogues with electron-rich quinone rings.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Robin B. Bedford, John G. Bowen, Amanda L. Weeks,