Articles citing this paper
Synthesis and Antineoplastic Activity of Quinoline Derivatives
Qiang Zhou A , Jing Hou A , Huamin Li A , Li Cui A , Han Jia A , Bing Gong A B and Lan He A C
+ Author Affiliations
- Author Affiliations
A Colleges of Chemistry and Resources Science and Technology, Beijing Normal University, Beijing 100875, China.
B Department of Chemistry, University at Buffalo, State University of New York, Buffalo, NY 14260, USA.
C Corresponding author. Email: helan1961@yahoo.com.cn
Australian Journal of Chemistry 61(7) 531-536 https://doi.org/10.1071/CH07419
Submitted: 5 December 2007 Accepted: 29 April 2008 Published: 16 July 2008
4 articles found in Crossref database.
Saccharomyces cerevisiae catalyzed one pot synthesis of isoindolo[2,1-a]quinazoline performed under ultrasonication
Avalani Jemin R.,
Patel Devji S., Raval Dipak K.
Journal of Molecular Catalysis B: Enzymatic. 2013 90 p.70
A Stereoselective Povarov Reaction Leading to exo‐Tetrahydroindolo[3,2‐c]quinoline Derivatives Catalyzed by Iodine
Wang Xiang‐Shan,
Yin Ming‐Yue,
Wang Wei, Tu Shu‐Jiang
European Journal of Organic Chemistry. 2012 2012(25). p.4811
Synthesis of 6-trifluoromethylindolo[1,2-c]quinazolines and related heterocycles using N-(2-iodophenyl)trifluoroacetimidoyl chlorides as starting material via C–H bond functionalization
Zhu Jiangtao,
Xie Haibo,
Chen Zixian,
Li Shan, Wu Yongming
Chem. Commun.. 2011 47(5). p.1512
Synthesis, β-haematin inhibition, and in vitro antimalarial testing of isocryptolepine analogues: SAR study of indolo[3,2-c]quinolines with various substituents at C2, C6, and N11
Wang Ning,
Wicht Kathryn J.,
Imai Kento,
Wang Ming-qi,
Anh Ngoc Tran,
Kiguchi Ryo,
Kaiser Marcel,
Egan Timothy J., Inokuchi Tsutomu
Bioorganic & Medicinal Chemistry. 2014 22(9). p.2629
