Department of Chemistry, Graduate School of Science , Tohoku University , 6-3 Aramaki-Aza , Aoba, Aoba-ku, Sendai , Miyagi 980-8578 , Japan.
Department of Industrial Chemistry, Faculty of Engineering , Tokyo University of Science , Kagurazaka, Shinjuku-ku , Tokyo 162-8601 , Japan.
Org Lett. 2018 Apr 20;20(8):2391-2394. doi: 10.1021/acs.orglett.8b00728. Epub 2018 Apr 4.
Prolinate salt is an efficient catalyst in the Mannich reaction of alkynyl imine and aldehyde, to afford synthetically useful chiral propargyl amine derivatives with excellent syn-selectivity and nearly perfect control of the absolute configuration. The counterion of the prolinate salt does not affect the enantioselectivity. This is a rare example, in which proline alkali metals, alkaline-earth metals, or ammonium salt show higher reactivity and better stereoselectivity than the parent proline.
脯氨酸盐是炔基亚胺和醛的曼尼希反应中的高效催化剂,可提供具有优异的 syn-选择性和近乎完美的绝对构型控制的合成有用的手性炔丙基胺衍生物。脯氨酸盐的反离子不影响对映选择性。这是一个罕见的例子,其中脯氨酸的碱金属、碱土金属或铵盐比母体脯氨酸表现出更高的反应性和更好的立体选择性。