A facile and efficient synthesis of hexahydro-1H-pyrido[2,3-b]indol-2-one scaffolds via a sequential Michael addition/amidation/reductive cyclization process

标题
A facile and efficient synthesis of hexahydro-1H-pyrido[2,3-b]indol-2-one scaffolds via a sequential Michael addition/amidation/reductive cyclization process
作者
关键词
Hexahydro-1, H, -pyrido[2,3-, b, ]indol-2-one, 3-Monosubstituted oxindole, Michael addition, Amidation, Reductive cyclization, Antitumor activity
出版物
TETRAHEDRON
Volume 71, Issue 50, Pages 9483-9495
出版商
Elsevier BV
发表日期
2015-10-24
DOI
10.1016/j.tet.2015.10.039

向作者/读者发起求助以获取更多资源

Reprint

联系作者

Discover Peeref hubs

Discuss science. Find collaborators. Network.

Join a conversation

Create your own webinar

Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.

Create Now