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Chiral bifunctional organocatalysts bearing a 1,3-propanediamine unit for the aza-MBH reaction
Authors:Shuichi Hirata  Kouichi Tanaka  Katsuya Matsui  Fernando Arteaga Arteaga  Yasushi Yoshida  Shinobu Takizawa  Hiroaki Sasai
Institution:The Institute of Scientific and Industrial Research (ISIR), Osaka University, Mihogaoka, Ibaraki, Osaka 567-0047, Japan
Abstract:The introduction of a 1,3-propanediamine unit at the 3-position of (S)-BINOL using a methylene spacer led to the formation of a chiral bifunctional organocatalyst for the aza-Morita–Baylis–Hillman (aza-MBH) reaction. The organocatalyst 1k mediated aza-MBH transformations with high chemical yields and with up to 82% ee.
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