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N-H carbazole synthesis from 2-chloroanilines via consecutive amination and C-H activation
Authors:Bedford Robin B  Betham Michael
Institution:School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK. r.bedford@bristol.ac.uk
Abstract:N-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-O-methylmukonal, and can be extended to the synthesis of indoles.
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