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Efficient Synthesis of 1-Aryl-1H-indazole Derivatives via Copper(I)-Catalyzed Intramolecular Amination Reaction

A copper(I)-catalyzed intramolecular amination reaction using CuI, KOH, and 1,4-dioxane at 105°C for the preparation of 1-aryl-1H-indazole derivatives was described. The method was applied to a wide scope of substrates and afforded indazole products in high yields.

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Published in:Synthetic communications 2008-01, Vol.38 (2), p.249-254
Main Authors: Liu, Rui, Zhu, Yongming, Qin, Liena, Ji, Shunjun
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container_title Synthetic communications
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creator Liu, Rui
Zhu, Yongming
Qin, Liena
Ji, Shunjun
description A copper(I)-catalyzed intramolecular amination reaction using CuI, KOH, and 1,4-dioxane at 105°C for the preparation of 1-aryl-1H-indazole derivatives was described. The method was applied to a wide scope of substrates and afforded indazole products in high yields.
doi_str_mv 10.1080/00397910701750250
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ispartof Synthetic communications, 2008-01, Vol.38 (2), p.249-254
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source Taylor and Francis Science and Technology Collection
subjects 1,10-phenanthroline
arylhydrazones
copper(I) iodide
indazole
intramolecular amination
title Efficient Synthesis of 1-Aryl-1H-indazole Derivatives via Copper(I)-Catalyzed Intramolecular Amination Reaction
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