Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter

Literature Information

Publication Date 2017-05-25
DOI 10.1039/C7QO00291B
Impact Factor 5.281
Authors

Bing Liu, Zhan-Ming Zhang, Bing Xu, Shan Xu, Hai-Hong Wu, Yuanyuan Liu, Junliang Zhang


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Abstract

A highly chemo-, diastereo-, and enantioselective Cu(I)/(S,S)-iPr-FOXAP-catalyzed Michael addition of ketiminoester to β-trifluoromethyl β,β-disubstituted enones was developed. This method provides facile access to highly functionalized 1-pyrrolines bearing two contiguous stereocenters, including a trifluoromethylated all-carbon quaternary stereocenter, via one-pot hydrolytic cyclization (up to >20 : 1 cr, > 20 : 1 dr, and 98% ee). The addition of trace amounts of water to the direct 1,3-dipolar cycloaddition is crucial for obtaining 1-pyrrolines with high chemoselectivities rather than pyrrolidines.

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Organic Chemistry Frontiers
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