Zhao Shi-Na, Li Qian, Qiao Xiu-Xiu, He Yonghui, Li Ganpeng, Zhao Xiao-Jing
Key Laboratory of Chemistry in Ethnic Medicinal Resources, Key Laboratory of Natural Products Synthetic Biology of Ethnic Medicinal Endophytes, State Ethnic Affairs Commission & Ministry of Education, School of Ethnic Medicine, Yunnan Minzu University, Kunming, 650500, China.
Chemistry. 2024 Dec 13;30(70):e202402843. doi: 10.1002/chem.202402843. Epub 2024 Nov 7.
The utilization of axially chiral biaryl diamines has been widely acknowledged as highly advantageous structures for the advancement of chiral catalysts and ligands. This highlights their extensive range of applications in asymmetric catalysis and synthesis. Herein, we devised a direct arylation reactions of 5-aminopyrazoles with azonaphthalenes, utilizing chiral phosphoric acid as the catalyst. This method delivers structurally novel atroposelective N, N-1,2-azole heteroaryl diamines with high yields (up to >98 %) and good to excellent enantiomeric ratios while exhibiting a wide range of substrate compatibility.
轴向手性联芳基二胺的应用已被广泛认可为用于开发手性催化剂和配体的极具优势的结构。这突出了它们在不对称催化和合成中的广泛应用范围。在此,我们设计了5-氨基吡唑与氮杂萘的直接芳基化反应,使用手性磷酸作为催化剂。该方法能以高产率(高达>98%)提供结构新颖的阻转选择性N,N-1,2-唑杂芳基二胺,对映体比例良好至优异,同时展现出广泛的底物兼容性。