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      Highly Regio-, Diastereo-, and Enantioselective Mannich Reaction of Allylic Ketones and Cyclic Ketimines: Access to Chiral Benzosultam.

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          Abstract

          An organocatalytic asymmetric Mannich reaction of allylic ketones with cyclic N-sulfonyl α-iminoester has been developed. By using a saccharide-derived chiral tertiary amino-thiourea catalyst, a range of allylic ketones and N-sulfonyl ketimines reacted smoothly to afford tetrasubstituted α-amino esters in high yields with good to excellent regio-, diastero-, and enantioselectivities.

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          Author and article information

          Journal
          Org Lett
          Organic letters
          American Chemical Society (ACS)
          1523-7052
          1523-7052
          Sep 18 2015
          : 17
          : 18
          Affiliations
          [1 ] Department of Chemistry, Tianjin University, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) , Tianjin 300072, P. R. of China.
          [2 ] State Key Laboratory of Elemento-Organic Chemistry, Nankai University , Tianjin 300071, P. R. of China.
          Article
          10.1021/acs.orglett.5b02351
          26335386
          c20af207-e9f2-4fb9-8896-44336b3ce8d5
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