Affiliation:
1. State Key Laboratory of Functions and Applications of Medicinal Plants Guizhou Medical University Guiyang 550014 P. R. China
2. Natural Products Research Center of Guizhou Province Guiyang 550014 P. R. China
Abstract
AbstractHerein, we report a general copper‐catalyzed method for the tunable oxygenative rearrangement of tetrahydrocarbazoles to cyclopentyl‐bearing spiroindolin‐2‐ones and spiroindolin‐3‐ones. The method demonstrates excellent chemoselectivity, regioselectivity, and product control simply by using the H2O and O2 as oxygen source, respectively. This open‐flask method is safe and simple to operate, and no other chemical oxidants are required. Besides, inspired from the unique pathway of 1, 2‐migration rearrangement, a highly controllable hydroxylation of indoles for the construction of C3a‐hydroxyl iminium indolines was also developed. Mechanistic experiments suggest that a single‐electron transfer‐induced oxidation process is responsible for the tunable selectivity control.
Funder
National Natural Science Foundation of China