<i>N</i>-H Carbazole Synthesis from 2-Chloroanilines via Consecutive Amination and C−H Activation Robin B. Bedford Michael Betham 10.1021/jo061749g.s001 https://acs.figshare.com/articles/journal_contribution/_i_N_i_H_Carbazole_Synthesis_from_2_Chloroanilines_via_Consecutive_Amination_and_C_H_Activation/3042769 <i>N</i>-H carbazoles can be produced from 2-chloroanilines and aryl bromides via consecutive catalytic amination and C−H activation. In many instances, this can be done in a tandem manner in one pot. The methodologies developed can be used in the synthesis of a range of carbazoles, including the natural products Clausine P and glycozolidine and a precursor in the synthesis of Clausines H, K, O, and 7-methoxy-<i>O</i>-methylmukonal, and can be extended to the synthesis of indoles. 2006-12-08 00:00:00 Consecutive Amination products Clausine P carbazole tandem manner Clausines H aryl bromides synthesis