Synthesis ( IF 2.6 ) Pub Date : 2017-09-25 , DOI: 10.1055/s-0036-1588566 Zhi-Zhen Huang 1 , Peng Bai 1 , Kenneth Huang 2
Abstract
A cascade C–H functionalization/C(sp3)–C(sp3) formation/cyclization reaction of N-methoxybenzamides with diazomalonates under rhodium(III) catalysis is developed for the efficient synthesis of isoquinolinedione derivatives. A plausible mechanism involving double migratory insertions of carbenes for the formation of C(sp2)–C(sp3) and C(sp3)–C(sp3) bonds by rhodium(III) catalysis is also proposed.
A cascade C–H functionalization/C(sp3)–C(sp3) formation/cyclization reaction of N-methoxybenzamides with diazomalonates under rhodium(III) catalysis is developed for the efficient synthesis of isoquinolinedione derivatives. A plausible mechanism involving double migratory insertions of carbenes for the formation of C(sp2)–C(sp3) and C(sp3)–C(sp3) bonds by rhodium(III) catalysis is also proposed.
中文翻译:
Rh(III)催化的级联C–H官能化/ C(sp3)–C(sp3)形成/环化反应合成异喹啉二酮衍生物
摘要
在铑(III)催化下,N-甲氧基苯甲酰胺与重氮丙二酸酯的级联C–H功能化/ C(sp 3)–C(sp 3)形成/环化反应被开发用于有效合成异喹啉二酮衍生物。还提出了一种可能的机制,该机制涉及通过铑(III)催化碳二烯双迁移插入形成C(sp 2)–C(sp 3)和C(sp 3)–C(sp 3)键。
在铑(III)催化下,N-甲氧基苯甲酰胺与重氮丙二酸酯的级联C–H功能化/ C(sp 3)–C(sp 3)形成/环化反应被开发用于有效合成异喹啉二酮衍生物。还提出了一种可能的机制,该机制涉及通过铑(III)催化碳二烯双迁移插入形成C(sp 2)–C(sp 3)和C(sp 3)–C(sp 3)键。