An efficient in-situ reduction and cyclization reaction for the synthesis of 9-aryl-1,6,8,9-tetrahydro-7 H -pyrazolo[3,4- f ]quinolin-7-one, 11-aryl-1,6,7,8,9,11-hexahydro-10 H -pyrazolo [3,4- a ]acridin-10-one, and 11-aryl-3,6,7,8,9,11-hexahydro-10 H -imidazo[4,5- a ]acridin-10-one derivatives
-
Published:2017-11
Issue:48
Volume:73
Page:6805-6814
-
ISSN:0040-4020
-
Container-title:Tetrahedron
-
language:en
-
Short-container-title:Tetrahedron
Author:
Yan Lirong,Li Qingyang,Xu Hui,Xu Zhongyun,Yu Qiuyu,Qin Yaqi,Rong Liangce
Funder
NSFC
Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials
Natural Science Research in Jiangsu Province
College students' innovative projects in jiangsu province
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference38 articles.
1. Comprehensive Heterocyclic Chemistry II;Jones,1996
2. Solid-phase synthesis of backbone-modified DNA analogs by the boranophosphotriester method using new protecting groups for nucleobases
3. 3-(1,1-Dioxo-2H-(1,2,4)-benzothiadiazin-3-yl)-4-hydroxy-2(1H)-quinolinones, Potent Inhibitors of Hepatitis C Virus RNA-Dependent RNA Polymerase
4. Hasegawa, S.; Matsunaga, K.; Muto, M.; Hanada, S.; JP Patent 02032086, 1990;
5. Identification and Specificity Studies of Small-Molecule Ligands for SH3 Protein Domains
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献