Journal
CHEMICAL COMMUNICATIONS
Volume 56, Issue 90, Pages 13963-13966Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc06490d
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Funding
- National Research Foundation of Korea (NRF) - Korea government (MSIT) [2012M3A7B404 9644, 2018R1A2A2A05018392, 2014-011165]
- National Research Foundation of Korea [2018R1A2A2A05018392] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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A highly effective and straightforward one-pot synthesis of diversely substituted 2-aminoindoles has been developed, involving sequential Au(I)-catalyzed regioselective hydroamination and CuCl2-mediated oxidative cyclization. This protocol offers an operationally easy, simple, robust, and sustainable approach with the use of readily available starting materials, good functional group tolerance, and high practicality and efficiency.
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