A concise synthesis of (+)-artemisinin.
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[1] J. Yadav,et al. A concise stereoselective total synthesis of (+)-artemisinin , 2010 .
[2] B. Stammen,et al. An approach to bufadienolides from deoxycholic acid. Reactions of a steroidal αβ-unsaturated aldehyde with some O-silylated ketene acetals , 1989 .
[3] Mitchell A. Avery,et al. The Total synthesis of (+)-artemisinin and (+)-9-desmethyltemesinin , 1987 .
[4] M. A. Kumar,et al. Stereoselective synthesis of artemisinin , 1990 .
[5] Xu Xing-xiang,et al. Total Synthesis of Arteannuin and Deoxyarteannuin. , 1986 .
[6] Paul A Wender,et al. Function-oriented synthesis, step economy, and drug design. , 2008, Accounts of chemical research.
[7] Yi Li,et al. The Genetic Map of Artemisia annua L. Identifies Loci Affecting Yield of the Antimalarial Drug Artemisinin , 2010, Science.
[8] J. Keasling,et al. Engineering a mevalonate pathway in Escherichia coli for production of terpenoids , 2003, Nature Biotechnology.
[9] Peter H Seeberger,et al. Continuous-flow synthesis of the anti-malaria drug artemisinin. , 2012, Angewandte Chemie.
[10] R. Shapiro,et al. Tosylhydrazones and alkyllithium reagents: More on the regiospecificity of the reaction and the trapping of three intermediates , 1975 .
[11] Richard Van Noorden. Demand for malaria drug soars , 2010, Nature.
[12] Jay D. Keasling,et al. High-Level Production of Amorpha-4,11-Diene, a Precursor of the Antimalarial Agent Artemisinin, in Escherichia coli , 2009, PloS one.
[13] H. W. Scheeren,et al. High pressure-promoted cycloadditions of ketene acetals and α,β-unsaturated aldehydes and ketones , 1985 .
[14] G. Jarugumilli,et al. Re-Evaluating the Nucleophilicity of Zinc Enolates in Alkylation Reactions† , 2012 .
[15] J. Aubry,et al. 90Mo NMR and kinetic studies of peroxomolybdic intermediates involved in the catalytic disproportionation of hydrogen peroxide by molybdate ions , 1995 .
[16] M. Jung,et al. Vinylsilanes as carbonyl precursors. Use in annelation reactions , 1974 .
[17] Timothy S. Ham,et al. Production of the antimalarial drug precursor artemisinic acid in engineered yeast , 2006, Nature.
[18] Jay D. Keasling,et al. Production of amorphadiene in yeast, and its conversion to dihydroartemisinic acid, precursor to the antimalarial agent artemisinin , 2012, Proceedings of the National Academy of Sciences.
[19] N. White,et al. Qinghaosu (Artemisinin): The Price of Success , 2008, Science.
[20] Wei-Shan Zhou,et al. Total Synthesis of the Antimalarial Sesquiterpene Peroxide Qinghaosu and Yingzhaosu A , 1994 .
[21] Jay D Keasling,et al. Engineering Escherichia coli for production of functionalized terpenoids using plant P450s. , 2007, Nature chemical biology.
[22] Hubert Lam,et al. A succinct method for preparing the Stork-Jung vinylsilane robinson annulation reagent. , 2005, The Journal of organic chemistry.
[23] J. Zukerman-Schpector,et al. A NOVEL ASYMMETRIC TOTAL SYNTHESIS OF (+)-ARTEMISININ , 1996 .
[24] J. Aubry,et al. Chemical sources of singlet oxygen. 2. Quantitative generation of singlet oxygen from hydrogen peroxide disproportionation catalyzed by molybdate ions , 1988 .
[25] Liu Hsing-Jang,et al. A total synthesis of the antimarial natural product (+)-qinghaosu , 1993 .
[26] G. Schmid,et al. Total synthesis of qinghaosu , 1983 .
[27] M. Avery,et al. Stereoselective total synthesis of (+)-artemisinin, the antimalarial constituent of Artemisia annua L , 1992 .