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    <description>Professor Krische's research focuses on the development of new synthetic methods with attendant applications in natural product synthesis. A central theme of his program involves the identification of new reactivity patterns, the evolution of related catalytic processes and, ultimately, the development of new synthetic strategies. His research program encompasses organic synthesis, catalysis, organometallic chemistry, and supramolecular chemistry.</description>
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      <title>H2-mediated C-C Coupling</title>
      <link>http://krische.cm.utexas.edu/research/krische/Research/Entries/2011/8/13_H2-mediated_C-C_Coupling.html</link>
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      <pubDate>Sat, 13 Aug 2011 17:25:08 -0500</pubDate>
      <description> </description>
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      <title>Natural Product Synthesis</title>
      <link>http://krische.cm.utexas.edu/research/krische/Research/Entries/2011/8/12_Natural_Product_Synthesis.html</link>
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      <pubDate>Fri, 12 Aug 2011 16:41:31 -0500</pubDate>
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      <title>Nucleophilic Catalysis</title>
      <link>http://krische.cm.utexas.edu/research/krische/Research/Entries/2011/3/22_Nucleophilic_Catalysis.html</link>
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      <pubDate>Tue, 22 Mar 2011 10:01:15 -0500</pubDate>
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      <title>Cat. Conj. Addition / Trapping</title>
      <link>http://krische.cm.utexas.edu/research/krische/Research/Entries/2011/3/21_Cat._Conj._Addition___Trapping.html</link>
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      <pubDate>Mon, 21 Mar 2011 00:00:00 -0500</pubDate>
      <description>&amp;quot;Desymmetrization of Enone-Diones via Rhodium Catalyzed Catalytic Diastereo- and Enantioselective Tandem Conjugate Addition-Aldol Cyclization&amp;quot; Bocknack, B. M.; Wang, L.-C.; Krische, M. J. Proc. Nat. Acad. Sci. 2004, 101, 5421.&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&amp;quot;Copper Catalyzed Tandem Conjugate Addition-Electrophilic Trapping: Ketones, Esters and Nitriles as Terminal Electrophiles&amp;quot; Agapiou, K.; Cauble, D. F.; Krische, M. J. J. Am. Chem. Soc. 2004, 126, 4528.&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&amp;quot;Diastereo- and Enantioselective Catalytic Carbometallative Aldol Cycloreduction: Tandem Conjugate Addition-Aldol Cyclization&amp;quot; Cauble, D. F.; Gipson, J. D.; Krische, M. J. J. Am. Chem. Soc. 2003, 125, 1110.&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;</description>
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      <title>Metal-Catalyzed [2+2] Cycloaddition</title>
      <link>http://krische.cm.utexas.edu/research/krische/Research/Entries/2011/3/20_Metal-Catalyzed_%5B2+2%5D_Cycloaddition.html</link>
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      <pubDate>Sun, 20 Mar 2011 00:00:00 -0500</pubDate>
      <description>&amp;quot;A Mechanistic Dichotomy in the Reaction of Gilman Reagents with Conjugated Enones: Partitioning of Electron Transfer and Conjugate Addition Manifolds&amp;quot; Yang, J.; Cauble, D. C.; Berro, A. J.; Bauld, N. L.; Krische, M. J. J. Org. Chem. 2004, 69, 7979.&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&amp;quot;Chemically Induced Anion Radical Cycloadditions: Intramolecular Cyclobutanation of bis(Enones) via Homogeneous Electron Transfer&amp;quot; Yang, J.; Felton, G. A. N.; Bauld, N. L.; Krische, M. J. J. Am. Chem. Soc. 2004, 126, 1634.&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&amp;quot;Diastereoselective Cycloreductions and Cycloadditions Catalyzed by Co(dpm)2/Silane (dpm = 2,2,6,6-tetramethyl-heptane-3,5-dionate): Mechanism and Partitioning of Hydrometallative vs. Anion Radical Pathways&amp;quot; Wang, L.-C.; Jang, H.-Y.; Roh, Y.; Schultz, A. J.; Wang, X.; Lynch, V.; Krische, M. J. J. Am. Chem. Soc. 2002, 124, 9448.&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&amp;quot;Anion Radical Chain Cycloaddition of Tethered Enones: Intramolecular Cyclobutanation and Diels-Alder Cycloaddition&amp;quot; Roh, Y.; Jang, H.-Y.; Bauld, N. L.; Krische, M. J. Org. Lett. 2002, 4, 611.&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&amp;quot;Diastereoselective Metal Catalyzed [2+2]Cycloaddition of Tethered Enones&amp;quot; Baik, T.-G.; Wang, L.-C.; Luiz, A.-L.; Krische, M. J. J. Am. Chem. Soc. 2001, 123, 6716.&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;&lt;br/&gt;</description>
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