Add time:07/14/2019 Source:sciencedirect.com
Treatment of 3-amidoindoles with phosphoryl chloride leads to a dimerization of the resulting iminochlorides to form tetrasubstituted imidazoles in moderate yield. One indole ring undergoes ring-opening to allow the formation of the imidazole ring. This strategically simple synthesis considerably expands the scope of delivering N-indolylimidazoles.
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