1049682-00-9Relevant academic research and scientific papers
Regioselective synthesis and in vitro anticancer activity of 4-aza-podophyllotoxin derivatives catalyzed by l -proline
Shi, Chunling,Wang, Juxian,Chen, Hui,Shi, Daqing
, p. 430 - 434 (2010)
A series of 4-aza-podophyllotoxin derivatives have been synthesized regioselectively via the three-component reaction of aldehydes, aromatic amines, and tetronic acid catalyzed by l-proline. This method has the advantages of high yield, high regioselectiv
An efficient microwave-assisted synthesis furo[3,4-b]-[4,7]phenanthroline and indeno[2,1-b][4,7]phenanthroline derivatives in water
Shi, Feng,Zhou, Dianxiang,Tu, Shujiang,Shao, Qingqing,Li, Chunmei,Cao, Longji
, p. 1065 - 1070 (2008/12/20)
(Chemical Equation Presented) A series of furo[3,4-b][4,7]phenanthroline and indeno[2,1-b][4,7]phenanthroline derivatives were synthesized via a three-component reaction of aromatic aldehydes, 6-aminoquinoline and either tetronic acid or 1,3-indanedione in water, under microwave irradiation without use of any catalyst. This green procedure offers several advantages including operational simplicity, clean reaction, and increased safety for small-scale high-speed synthesis.
