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		<title>Admin at 05:38, 22 August 2008</title>
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		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;AN   &lt;br /&gt;
     2006:21112  DISSABS   Order Number: AAI3185209&lt;br /&gt;
TI   &lt;br /&gt;
     ROMP approaches for organic synthesis and efforts toward the synthesis of&lt;br /&gt;
     cyclipostins&lt;br /&gt;
AU   &lt;br /&gt;
     Poon, Wing Cheong [Ph.D.]; Hanson, Paul R. [advisor]&lt;br /&gt;
CS   &lt;br /&gt;
     The University of Kansas (0099)&lt;br /&gt;
SO   &lt;br /&gt;
     Dissertation Abstracts International, (2004) Vol. 66, No. 8B, p. 4231.&lt;br /&gt;
     Order No.: AAI3185209. 155 pages. &lt;br /&gt;
     ISBN: 0-542-26785-3.&lt;br /&gt;
DT   &lt;br /&gt;
     Dissertation&lt;br /&gt;
FS   &lt;br /&gt;
     DAI&lt;br /&gt;
LA   &lt;br /&gt;
     English&lt;br /&gt;
ED   &lt;br /&gt;
     Entered STN: 20060428&lt;br /&gt;
     Last Updated on STN: 20060428&lt;br /&gt;
AB   &lt;br /&gt;
          The work reported herein describes the applications of ring-opening&lt;br /&gt;
     metathesis polymerization (ROMP) using well-defined ruthenium-based&lt;br /&gt;
     catalysts for organic synthesis, and efforts toward the synthesis of&lt;br /&gt;
     cyclipostins.&lt;br /&gt;
          A strategy to synthesize oligomeric sulfonamides employed both&lt;br /&gt;
     ring-closing metathesis (RCM) and ring-opening metathesis polymerization&lt;br /&gt;
     (ROMP). Amino acid-derived cyclic sulfonamides containing either exocyclic&lt;br /&gt;
     or γ-endocyclic stereogenic centers were generated via RCM. These&lt;br /&gt;
     cyclic sulfonamides underwent stereoselective Diels-Alder reactions to&lt;br /&gt;
     yield endo-norbornenyl sulfonamides as major diastereomers. Subsequent&lt;br /&gt;
     ROMP rapidly produced sulfonamide-based oligomers, and these oligomers&lt;br /&gt;
     exhibited different solubility in a variety of solvents. Based on the&lt;br /&gt;
     solubility difference of these oligomers, a capture-ROMP-release strategy&lt;br /&gt;
     for the chromatography-free purification of Mitsunobu reaction products is&lt;br /&gt;
     described. Oxo-norbornenyl-tagged reagents are utilized for standard&lt;br /&gt;
     solution phase Mitsunobu chemistry. Post-reaction, phase-switching was&lt;br /&gt;
     accomplished via in situ ROMP followed by precipitation of the polymer&lt;br /&gt;
     with methanol. Release of the product from the polymer afforded amines and&lt;br /&gt;
     alkyl hydrazine derivatives with good yields and purities.&lt;br /&gt;
          The C-H activation strategy mediated by Rh2(OAc)4 was utilized toward&lt;br /&gt;
     the synthesis of cyclipostins. This novel class of natural product&lt;br /&gt;
     possesses strong inhibitory action against hormone-sensitive lipase&lt;br /&gt;
     (HSL) and has potential in the development of therapeutic agents to&lt;br /&gt;
     regulate lipolysis for the treatment of noninsulin-dependent diabetes&lt;br /&gt;
     mellitus (NIDDM). The initial results of this project are reported.&lt;br /&gt;
CC   &lt;br /&gt;
     0490 CHEMISTRY, ORGANIC; 0487 CHEMISTRY, BIOCHEMISTRY&lt;/div&gt;</summary>
		<author><name>Admin</name></author>	</entry>

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