Highly Regio‑, Diastereo‑, and Enantioselective Mannich Reaction of Allylic Ketones and Cyclic Ketimines: Access to Chiral Benzosultam
收藏Figshare2016-02-13 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Highly_Regio_Diastereo_and_Enantioselective_Mannich_Reaction_of_Allylic_Ketones_and_Cyclic_Ketimines_Access_to_Chiral_Benzosultam/2130523
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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.
创建时间:
2016-02-13



