92855-33-9Relevant articles and documents
Chiral Br?nsted Acid Catalyzed Dynamic Kinetic Asymmetric Hydroamination of Racemic Allenes and Asymmetric Hydroamination of Dienes
Lin, Jin-Shun,Li, Tao-Tao,Jiao, Guan-Yuan,Gu, Qiang-Shuai,Cheng, Jiang-Tao,Lv, Ling,Liu, Xin-Yuan
supporting information, p. 7092 - 7096 (2019/04/26)
The first highly efficient and practical chiral Br?nsted acid catalyzed dynamic kinetic asymmetric hydroamination (DyKAH) of racemic allenes and asymmetric hydroamination of unactivated dienes with both high E/Z selectivity and enantioselectivity are described herein. The transformation proceeds through a new catalytic asymmetric model involving a highly reactive π-allylic carbocationic intermediate, generated from racemic allenes or dienes through a proton transfer mediated by an activating/directing thiourea group. This method affords expedient access to structurally diverse enantioenriched, potentially bioactive alkenyl-containing aza-heterocycles and bicyclic aza-heterocycles.
Search for new Ca++ antagonists. Lipophilic oximes and phosphonates
Bellucci,Teodori,Gualtieri
, p. 730 - 744 (2007/10/02)
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