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Stereoselective 1,3-Dipolar Cycloadditions of Photochemically Generated Azomethine Ylides to Oppolzer's Chiral Acryloyl Sultam. An Asymmetric Approach to Quinocarcin
Garner, Philip,Ho, Wen Bin
, p. 3973 - 3975 (1990)
Photochemically generated azomethine ylides undergo highly stereoselective 1,3-dipolar cycloadditions (ds >25:1) to chiral acryloyl sultams to give the substituted 3,8-diazabicyclooctane moiety of quinocarcin.
