期刊
CHEMICAL COMMUNICATIONS
卷 56, 期 93, 页码 14617-14620出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc05862a
关键词
-
资金
- National Natural Science Foundation of China [21901187, 21672164, 21372177]
A straightforward and efficient method for the preparation of 2-aryl-2H-indazoles from ortho-alkyl substituted azoxybenzenes is presented. The reaction proceeds through base-catalyzed benzyl C-H deprotonation and cyclization to afford 2-aryl-2H-indazoles in good yields. This synthetic strategy can be applied to the construction of several fluorescent and bioactive molecules.
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