Zhang Lijun, Song Zhiguang
College of Chemistry, Jilin University, Changchun, Jilin 130012, P. R. China.
Org Lett. 2024 Mar 22;26(11):2192-2196. doi: 10.1021/acs.orglett.4c00294. Epub 2024 Mar 8.
Herein we present a facile and efficient one-pot synthetic protocol for the construction of polycyclic sultams. This protocol involves gold-catalyzed intramolecular hydroamination of -alkynylbenzenesulfonamides followed by HTIB-mediated counteranion-assisted intramolecular annulation. The transformation tolerates a wide range of functional groups, resulting in the formation of highly functionalized and valuable polycyclic sultam skeletons in moderate to excellent yields. These polycyclic sultams are widely used as key building blocks in organic science.
在此,我们提出了一种简便高效的一锅法合成多环磺内酰胺的方案。该方案包括金催化的α-炔基苯磺酰胺的分子内氢胺化反应,随后是HTIB介导的抗衡阴离子辅助分子内环化反应。该转化反应能耐受多种官能团,以中等至优异的产率形成高度官能化且有价值的多环磺内酰胺骨架。这些多环磺内酰胺在有机科学中广泛用作关键结构单元。