Synthesis and Herbicidal Activity Evaluation of Novel β-Carboline Derivatives
Q Weng, J Huang, Y Zeng, Y Deng, M Hu
Index: Weng, Qunfang; Huang, Jingfei; Zeng, Yong; Deng, Yueye; Hu, Meiying Molecules, 2012 , vol. 17, # 4 p. 3969 - 3980
Full Text: HTML
Citation Number: 3
Abstract
Abstract: Based on the original structure of harmine, several novel 1, 2, 3, 4-tetrahydro-β- carboline, β-carboline and 1-substituted-β-carboline derivatives bearing a substituted carbohydrazide group at C-3 were designed and synthesized to investigate the structure- activity relationship of their analogues. All of the compounds were characterized by infrared (IR), proton and carbon nuclear magnetic resonance (1 H-NMR, 13 C-NMR), and mass ...
Related Articles:
[Cao, Rihui; Peng, Wenlie; Chen, Hongsheng; Hou, Xuerui; Guan, Huaji; Chen, Qi; Ma, Yan; Xu, Anlong European Journal of Medicinal Chemistry, 2005 , vol. 40, # 3 p. 249 - 257]
[Dong, Jing; Shi, Xiao-Xin; Yan, Jing-Jing; Xing, Jing; Zhang, Qiang; Xiao, Sen European Journal of Organic Chemistry, 2010 , # 36 p. 6987 - 6992]
[Cao, Rihui; Peng, Wenlie; Chen, Hongsheng; Hou, Xuerui; Guan, Huaji; Chen, Qi; Ma, Yan; Xu, Anlong European Journal of Medicinal Chemistry, 2005 , vol. 40, # 3 p. 249 - 257]
[Salvi; Choughuley Indian Journal of Chemistry - Section B Organic Chemistry Including Medicinal Chemistry, 1990 , vol. 29, # 10 p. 986 - 988]
Synthesis and antitumor activity of β-carboline 3-(substituted-carbohydrazide) derivatives
[Barbosa, Valeria Aquilino; Formagio, Anelise S. Nazari; Savariz, Franciele Cristina; Foglio, Mary Ann; Spindola, Humberto Moreira; De Carvalho, Joao Ernesto; Meyer, Emerson; Sarragiotto, Maria Helena Bioorganic and Medicinal Chemistry, 2011 , vol. 19, # 21 p. 6400 - 6408]