Garg Yuvraj, Osborne James, Vasylevskyi Serhii, Velmurugan Nivedha, Tanaka Fujie
Chemistry and Chemical Bioengineering Unit, Okinawa Institute of Science and Technology Graduate University, 1919-1 Tancha, Onna, Okinawa 904-0495, Japan.
Research Support Division, Okinawa Institute of Science and Technology Graduate University, 1919-1 Tancha, Onna, Okinawa 904-0495, Japan.
J Org Chem. 2023 Aug 4;88(15):11096-11101. doi: 10.1021/acs.joc.3c01051. Epub 2023 Jul 17.
1,3-Diamine-derived catalysts were designed, synthesized, and used in asymmetric Mannich reactions of ketones. The reactions catalyzed by one of the 1,3-diamine derivatives in the presence of acids afforded the Mannich products with high enantioselectivities under mild conditions. In most cases, bond formation occurred at the less-substituted α-position of the ketone carbonyl group. Our results indicate that the primary and the tertiary amines of the 1,3-diamine derivative cooperatively act for the catalysis.
设计、合成了1,3 -二胺衍生的催化剂,并将其用于酮的不对称曼尼希反应。其中一种1,3 -二胺衍生物在酸存在下催化的反应,在温和条件下能以高对映选择性得到曼尼希产物。在大多数情况下,键的形成发生在酮羰基取代较少的α-位。我们的结果表明,1,3 -二胺衍生物的伯胺和叔胺协同作用于催化反应。