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Pure Appl. Chem., 1998, Vol. 70, No. 3, pp. 539-546

http://dx.doi.org/10.1351/pac199870030539

The chemistry-medicine continuum: Synthetic, computer, spectroscopic and biological studies on new chemotherapeutic leads

Paul A. Wender, Yolanda Martin-Cantalejo, Andrew J. Carpenter, Anna Chiu, Jef De Brabander, Patrick G. Harran, Juan-Miguel Jimenez, Michael F. T. Koehler, Blaise Lippa, James A. Morrison, Stephan G. Müller, Stephan N. Müller, Cheol-Min Park, Makoto Shiozaki, Carsten Siedenbiedel, Donald J. Skalitzky, Masahiro Tanaka and Kazuhiro Irie

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  • Ylijoki Kai E. O., Stryker Jeffrey M.: [5 + 2] Cycloaddition Reactions in Organic and Natural Product Synthesis. Chem. Rev. 2013, 113, 2244. <http://dx.doi.org/10.1021/cr300087g>
  • Lu Yu, Woo Sang Kook, Krische Michael J.: Total Synthesis of Bryostatin 7 via C–C Bond-Forming Hydrogenation. J Ann Chem Soc 2011, 133, 13876. <http://dx.doi.org/10.1021/ja205673e>
  • Singh Vishwakarma, Murali Krishna Urlam, Vikrant, Trivedi Girish K.: Cycloaddition of oxidopyrylium species in organic synthesis. Tetrahedron 2008, 64, 3405. <http://dx.doi.org/10.1016/j.tet.2008.01.049>
  • 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>
  • Hilinski Michael K., Mayweg Alexander V. W., Wender Paul A.: Late-Stage Intermolecular CH Activation for Lead Diversification:  A Highly Chemoselective Oxyfunctionalization of the C-9 Position of Potent Bryostatin Analogues. Org Lett 2005, 7, 79. <http://dx.doi.org/10.1021/ol047859w>
  • VanDeusen Christopher L., Wender Paul A., Mayweg Alexander V. W.: A Concise, Selective Synthesis of the Polyketide Spacer Domain of a Potent Bryostatin Analogue. Org Lett 2003, 5, 277. <http://dx.doi.org/10.1021/ol0272390>
  • Kostensenker. Bryostatine und ihre Analoga. Nachr Chem Tech Lab 1999, 47, 432. <http://dx.doi.org/10.1002/nadc.19990470424>