Stereoselective synthesis of benzosulfamidate-fused tetrahydroquinazoline scaffold via organocatalytic [4+2] cycloaddition of 2-amino-β-nitrostyrenses of cyclic N-sulfimines
Concise synthesis of benzosulfamidate-fused tetrahydroquinazolines is developed. The method involves [4+2] cycloaddition reaction of o-N-Cbz-amino-β-nitrostyrene. Asymmetric [4+2] cycloaddition reaction is achieved.