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In this report, a mild and efficient method of 2-substituted indazolones via B2(OH)4-mediated reductive N-N bond formation is created. This strategy features moderate problems, no request for a metal catalyst, and a broad scope both for aliphatic and fragrant amines. Meanwhile, this method was additional successfully used on DNA to construct indazolone cores for a DNA-encoded collection. This may allow the creation of a very appealing indazolone-cored library from quick ami
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