Academic literature on the topic 'Auripyrone'
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Journal articles on the topic "Auripyrone"
Lister, Troy, and Michael V. Perkins. "Total Synthesis of Auripyrone A." Angewandte Chemie International Edition 45, no. 16 (April 10, 2006): 2560–64. http://dx.doi.org/10.1002/anie.200504573.
Full textLister, Troy, and Michael V. Perkins. "Total Synthesis of Auripyrone A." Angewandte Chemie 118, no. 16 (April 10, 2006): 2622–26. http://dx.doi.org/10.1002/ange.200504573.
Full textHayakawa, Ichiro, Takuma Takemura, Emi Fukasawa, Yuta Ebihara, Natsuki Sato, Takayasu Nakamura, Kiyotake Suenaga, and Hideo Kigoshi. "Total Synthesis of Auripyrones A and B and Determination of the Absolute Configuration of Auripyrone B." Angewandte Chemie International Edition 49, no. 13 (February 23, 2010): 2401–5. http://dx.doi.org/10.1002/anie.200906662.
Full textHayakawa, Ichiro, Takuma Takemura, Emi Fukasawa, Yuta Ebihara, Natsuki Sato, Takayasu Nakamura, Kiyotake Suenaga, and Hideo Kigoshi. "Total Synthesis of Auripyrones A and B and Determination of the Absolute Configuration of Auripyrone B." Angewandte Chemie 122, no. 13 (February 23, 2010): 2451–55. http://dx.doi.org/10.1002/ange.200906662.
Full textPerkins, Michael V., Saba Jahangiri, and Max R. Taylor. "Stereoselective synthesis of a novel spiroacetal-dihydropyrone related to auripyrone." Tetrahedron Letters 47, no. 12 (March 2006): 2025–28. http://dx.doi.org/10.1016/j.tetlet.2006.01.045.
Full textJung, Michael E., and Ramin Salehi-Rad. "Dipyrone approach toward the synthesis of the cytotoxic natural product auripyrone A." Tetrahedron Letters 51, no. 38 (September 2010): 4931–33. http://dx.doi.org/10.1016/j.tetlet.2010.07.034.
Full textPerkins, Michael V., Rebecca A. Sampson, John Joannou, and Max R. Taylor. "Stereoselective synthesis and cyclisation of the acyclic precursor to auripyrone A and B." Tetrahedron Letters 47, no. 22 (May 2006): 3791–95. http://dx.doi.org/10.1016/j.tetlet.2006.03.096.
Full textJung, Michael E., Manon Chaumontet, and Ramin Salehi-Rad. "Total Synthesis of Auripyrone B Using a Non-Aldol Aldol−Cuprate Opening Process." Organic Letters 12, no. 12 (June 18, 2010): 2872–75. http://dx.doi.org/10.1021/ol100985n.
Full textJung, Michael E., Manon Chaumontet, and Ramin Salehi-Rad. "ChemInform Abstract: Total Synthesis of Auripyrone B Using a Non-Aldol Aldol-Cuprate Opening Process." ChemInform 41, no. 44 (October 7, 2010): no. http://dx.doi.org/10.1002/chin.201044210.
Full textJung, Michael E, and Ramin Salehi-Rad. "Total Synthesis of Auripyrone A Using a Tandem Non-Aldol Aldol/Paterson Aldol Process as a Key Step." Angewandte Chemie International Edition 48, no. 46 (November 2, 2009): 8766–69. http://dx.doi.org/10.1002/anie.200904607.
Full textDissertations / Theses on the topic "Auripyrone"
Salehi-Rad, Ramin. "Total synthesis of auripyrone A." Diss., Restricted to subscribing institutions, 2009. http://proquest.umi.com/pqdweb?did=1973896461&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.
Full textLister, Troy, and mike perkins@flinders edu au. "Total Synthesis of Auripyrone A and Related Metabolites." Flinders University. School of Chemistry, Physics and Earth Sciences, 2006. http://catalogue.flinders.edu.au./local/adt/public/adt-SFU20060804.125858.
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