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Published on: July 28, 2022
Organocatalytic Enantioselective Aza-Michael Addition of N-Methoxyamides to α,β-Unsaturated Aldehydes
Chanhyun Jung1, Hyeju Jo1, Jae Sang Han1
1College of Pharmacy and Medicinal Research Center (MRC), Chungbuk National University, Cheongju 28160, Republic of Korea.
Abstract:
A highly enantioselective aza-Michael addition of N-methoxyamides to α,β-unsaturated aldehydes has been developed under organocatalytic conditions by using a Jørgensen-type pyrrolidine catalyst. The reaction affords β-amino carbonyl compounds with up to 97% ee in good to excellent yields. The resulting aza-Michael adducts can be readily transformed into 1,3-amino alcohols and 3,6-disubstituted 2-piperidones, which are valuable pharmacophores in medicinal chemistry.
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