Pure and Applied Chemistry

CrossRef Cited-by Linking

• Major Dan Thomas, Freud Yehoshua, Weitman Michal: Catalytic control in terpenoid cyclases: multiscale modeling of thermodynamic, kinetic, and dynamic effects. Current Opinion in Chemical Biology 2014, 21, 25. <http://dx.doi.org/10.1016/j.cbpa.2014.03.010>
• Kodet John G., Topczewski Joseph J., Gardner Kevyn D., Wiemer David F.: Electrophilic aromatic prenylation via cascade cyclization. Tetrahedron 2013, 69, 9212. <http://dx.doi.org/10.1016/j.tet.2013.08.056>
• Chen Mengbin, Al-lami Naeemah, Janvier Marine, D’Antonio Edward L., Faraldos Juan A., Cane David E., Allemann Rudolf K., Christianson David W.: Mechanistic Insights from the Binding of Substrate and Carbocation Intermediate Analogues to Aristolochene Synthase. Biochemistry 2013, 52, 5441. <http://dx.doi.org/10.1021/bi400691v>
• Köksal Mustafa, Chou Wayne K. W., Cane David E., Christianson David W.: Unexpected Reactivity of 2-Fluorolinalyl Diphosphate in the Active Site of Crystalline 2-Methylisoborneol Synthase. Biochemistry 2013, 52, 5247. <http://dx.doi.org/10.1021/bi400797c>
• Azam Muhammad, Song Min, Fan Fangjuan, Zhang Bo, Xu Yaying, Xu Changjie, Chen Kunsong: Comparative Analysis of Flower Volatiles from Nine Citrus at Three Blooming STAGES. IJMS 2013, 14, 22346. <http://dx.doi.org/10.3390/ijms141122346>
• Köksal Mustafa, Chou Wayne K. W., Cane David E., Christianson David W.: Structure of 2-Methylisoborneol Synthase from Streptomyces coelicolor and Implications for the Cyclization of a Noncanonical C-Methylated Monoterpenoid Substrate. Biochemistry (Wash ) 2012, 51, 3011. <http://dx.doi.org/10.1021/bi201827a>
• Köksal Mustafa, Chou Wayne K. W., Cane David E., Christianson David W.: Structure of Geranyl Diphosphate C-Methyltransferase from Streptomyces coelicolor and Implications for the Mechanism of Isoprenoid Modification. Biochemistry (Wash ) 2012, 51, 3003. <http://dx.doi.org/10.1021/bi300109c>
• Thibodeaux Christopher J., Chang Wei-chen, Liu Hung-wen: Enzymatic Chemistry of Cyclopropane, Epoxide, and Aziridine Biosynthesis. Chemistry Review 2012, 112, 1681. <http://dx.doi.org/10.1021/cr200073d>
• Major Dan Thomas, Weitman Michal: Electrostatically Guided Dynamics—The Root of Fidelity in a Promiscuous Terpene Synthase?. J. Am. Chem. Soc. 2012, 134, 19454. <http://dx.doi.org/10.1021/ja308295p>
• Pronin Sergey V., Shenvi Ryan A.: Synthesis of highly strained terpenes by non-stop tail-to-head polycyclization. Nature Chem 2012, 4, 915. <http://dx.doi.org/10.1038/nchem.1458>
• Faraldos Juan A., Gonzalez Veronica, Allemann Rudolf K.: The role of aristolochene synthase in diphosphate activation. Chem Commn 2012, 48, 3230. <http://dx.doi.org/10.1039/c2cc17588f>
• Ueberbacher Barbara T., Hall Mélanie, Faber Kurt: Electrophilic and nucleophilic enzymatic cascade reactions in biosynthesis. Natural Products Report 2012, 29, 337. <http://dx.doi.org/10.1039/c2np00078d>
• Jindal Garima, Sunoj Raghavan B.: Revisiting sesquiterpene biosynthetic pathways leading to santalene and its analogues: a comprehensive mechanistic study. Org. Biomol. Chem. 2012, 10, 7996. <http://dx.doi.org/10.1039/c2ob26027a>
• Faraldos Juan A., González Verónica, Senske Michael, Allemann Rudolf K.: Templating effects in aristolochene synthase catalysis: elimination versus cyclisation. Biomol Chem 2011, 9, 6920. <http://dx.doi.org/10.1039/c1ob06184d>
• Miller David J., Yu Fanglei, Knight David W., Allemann Rudolf K.: 6- and 14-Fluoro farnesyl diphosphate: mechanistic probes for the reaction catalysed by aristolochene synthase. Org Biomol Chem 2009, 7, 962. <http://dx.doi.org/10.1039/b817194g>