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Pure Appl. Chem., 2005, Vol. 77, No. 1, pp. 103-117

http://dx.doi.org/10.1351/pac200577010103

Approaches to the stereoselective total synthesis of biologically active natural products

Anne Baron, Matthew Ball, Benjamin Bradshaw, Sam Donnelly, Olivier Germay, Pilar C. Oller, Naresh Kumar, Nathaniel Martin, Matthew O’Brien, Hiroki Omori, Christopher Moore and Eric J. Thomas*

Department of Chemistry, University of Manchester, Manchester, M13 9PL, UK

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  • Trost Barry M., Yang Hanbiao, Brindle Cheyenne S., Dong Guangbin: Atom-Economic and Stereoselective Syntheses of the Ring A and B Subunits of the Bryostatins. Chemistry A European Journal 2011, 17, 9777. <http://dx.doi.org/10.1002/chem.201002930>
  • Fischer Petra, Gruner Margit, Jäger Anne, Kataeva Olga, Metz Peter: Total Synthesis of Pamamycin-649B. Chemistry A European Journal 2011, 17, 13334. <http://dx.doi.org/10.1002/chem.201102093>
  • Hale Karl J., Manaviazar Soraya: New Approaches to the Total Synthesis of the Bryostatin Antitumor Macrolides. Chem Asian J 2010, 5, 704. <http://dx.doi.org/10.1002/asia.200900634>
  • Cho Chang-Woo, Krische Michael J.: Enantioselective Reductive Coupling of Alkynes and α-Keto Aldehydes via Rhodium-Catalyzed Hydrogenation:  An Approach to Bryostatin Substructures. Org Lett 2006, 8, 891. <http://dx.doi.org/10.1021/ol052976s>
  • Baron Anne, Ball Matthew, Bradshaw Benjamin, Donnelly Sam, Germany Olivier, Oller Pilar C., Kumar Naresh, Martin Nathaniel, O'Brien Matthew, Omori Hiroki: Approaches to the Stereoselective Total Synthesis of Biologically Active Natural Products. ChemInform 2005, 36. <http://dx.doi.org/10.1002/chin.200535282>