A catalytic asymmetric Michael reaction using Schiff bases promoted by D 2 -symmetrical ammonium salts as phase-transfer catalysts is described.The reaction of glycine Schiff base (1a) gave the Michael adduct with up to 91% ee and tetrasubstituted carbons was also constructed using alanine Schiff base (3a) with up to 63% ee.
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Arai et al. (2006) studied this question.
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