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Molecular Diversity|March 16, 2010
Facile synthesis of indole- or benzofuran-fused benzo[a]carbazole-1,4-diones using a tandem two-step reaction sequenceShanghui Tu, Chunyong Ding, Wenxiang Hu, et al.
Molecular Diversity|March 16, 2010
Quantitative structure-activity relationship study of antitubercular fluoroquinolonesNikola Minovski, Marjan Vračko, Tom Solmajer
Molecular Diversity|April 26, 2017
FeCl₃-catalyzed [3+3] annulation between 3-oxirane-indolin-2-ones and nitrones to construct spiro[1,4,2-dioxazinan]oxindolesJingmiao Yu, Chun Cai
Molecular Diversity|June 28, 2018
Synthesis, in vitro [Formula: see text]-glucosidase inhibitory activity, and in silico study of (E)-thiosemicarbazones and (E)-2-(2-(arylmethylene)hydrazinyl)-4-arylthiazole derivativesMuhammad Ali, Khalid Mohammed Khan, Uzma Salar, et al.
Molecular Diversity|June 28, 2018
Highly efficient synthesis of alkyl and aryl primary thiocarbamates and dithiocarbamates under metal- and solvent-free conditionsAli Reza Sardarian, Iman Dindarloo Inaloo, Ali Reza Modarresi-Alam
Molecular Diversity|July 1, 2018
Insights into the interaction and binding mode of a set of antifungal azoles as inhibitors of potential fungal enzyme-based targetsCamilo Guerrero-Perilla, Freddy A Bernal, Ericsson Coy-Barrera
Molecular Diversity|July 5, 2018
QEX: target-specific druglikeness filter enhances ligand-based virtual screeningMasahiro Mochizuki, Shogo D Suzuki, Keisuke Yanagisawa, et al.
Molecular Diversity|July 6, 2018
Synthesis and biological evaluation of novel SIPI-7623 derivatives as farnesoid X receptor (FXR) antagonistsSi-Yun Nian, Guo-Ping Wang, Zheng-Li Jiang, et al.
Molecular Diversity|June 29, 2018
Synthesis of some new triamide derivatives via Ugi five-component reaction in aqueous solutionAli Asghar Mohammadi, Salman Taheri, Arman Amini, et al.
Molecular Diversity|January 15, 2010
A regiospecific synthesis of both positional isomers of 4,6-disubstituted 2-dicyanomethylene-1, 2-dihydropyridin-3-carbonitrilesFrancisco Carrión, Sofia H Pettersson, Jordi Rifá, et al.
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