Tang Shengbiao, Li Ziyong, Shao Ying, Sun Jiangtao
Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering , Changzhou University , 1 Gehu Road , 213164 , Changzhou , China.
Org Lett. 2019 Sep 20;21(18):7228-7232. doi: 10.1021/acs.orglett.9b02435. Epub 2019 Sep 11.
An unprecedented regio-controllable allylic amination of unactivated dienyl and trienyl allylic alcohols has been developed, providing an efficient approach toward the site-selective formation of C1-, C3-, and C5-/C7-amination products from the sole substrates. Key to this protocol is the use of secondary amines as the amination reagents, as well as the presence of an iridium catalyst and scandium triflate.
一种前所未有的未活化二烯基和三烯基烯丙醇的区域可控烯丙基胺化反应已被开发出来,为从单一底物位点选择性形成C1-、C3-和C5-/C7-胺化产物提供了一种有效方法。该方案的关键是使用仲胺作为胺化试剂,以及铱催化剂和三氟甲磺酸钪的存在。