Journal
CHEMICAL COMMUNICATIONS
Volume 53, Issue 6, Pages 1084-1087Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6cc09595j
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Funding
- National Natural Science Foundation of China [21372084, 21425205]
- MOE (PCSIRT)
- 973 Programs [2015CB-856600]
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A highly efficient tandem hydroamination and cyclization reaction of 2-trifluoromethyl-1,3-enynes with primary amines leading to 4-trifluoromethyl-3-pyrrolines was developed by using AgNO3 as a catalyst undermild reaction conditions. This newmethod is compatible with alkyl, aryl, and allyl primary amines, representing an atomeconomical protocol for the construction of 4-trifluoromethyl-3pyrrolines for the first time.
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