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<journal-id journal-id-type="publisher">global-journal-of-science-frontier-research-b-chemistry</journal-id>
<journal-title-group>
<journal-title>Global Journal of Science Frontier Research - B: Chemistry</journal-title>
</journal-title-group>
<issn publication-format="print">0975-5896</issn>
<issn publication-format="electronic">2249-4626</issn>
<publisher><publisher-name>Global Journals Publishing Group Incorporated</publisher-name></publisher>
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<article-id pub-id-type="publisher-id">76191</article-id>
<title-group>
<article-title>Synthesis of 6,6-Dimethyl-2-Cyclopentadienylethylbicyclo[3.1.1] Hept-2-Ene and of 6,6-Dimethyl-2-Indenylethylbicyclo[3.1.1] Hept-2-Ene.</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author"><name><surname>obuzor</surname><given-names>gloria</given-names></name><xref ref-type="aff" rid="aff1" />
</contrib>
</contrib-group>
<aff id="aff1">NIGERIA, University of Port Harcourt</aff>
<pub-date publication-format="electronic" date-type="pub" iso-8601-date="2013-06-26">
<day>26</day>
<month>06</month>
<year>2013</year>
</pub-date>
<volume>13</volume>
<issue>B5</issue>
<fpage>9</fpage>
<lpage>12</lpage>
<abstract><p>The new compounds 6,6-dimethyl-2-cyclopentadienylethylbicyclo[3.1.1] hept-2-ene (4) and 6,6-dimethyl-2-indenylethylbicyclo[3.1.1] hept-2-ene (5) were synthesized in 82% and 60% yield respectively using 6,6-dimethyl-2-p-toluenesulphonyloxomethylbicyclo[3.1.1] hept-2-ene (2). However, compounds -(4) and (5) were obtained in 71% and 81% yield respectively using 6,6-dimethyl-2-sulphonyloxomethylbicyclo[3.1.1] hept-2-ene (3). All compounds were characterized by NMR, Infra-red, Micro Analysis and Mass Spectroscopy.</p></abstract>
<kwd-group kwd-group-type="author-generated">
<kwd>ligand</kwd>
<kwd>metallocene</kwd>
<kwd>cyclopentadienyl</kwd>
<kwd>indenyl</kwd>
<kwd>organ metallic</kwd>
<kwd>n-buthyllithium.</kwd>
</kwd-group>
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<title>Full Text</title>
<p>The new compounds 6,6-dimethyl-2-cyclopentadienylethylbicyclo[3.1.1] hept-2-ene (4) and 6,6-dimethyl-2-indenylethylbicyclo[3.1.1] hept-2-ene (5) were synthesized in 82% and 60% yield respectively using 6,6-dimethyl-2-p-toluenesulphonyloxomethylbicyclo[3.1.1] hept-2-ene (2). However, compounds -(4) and (5) were obtained in 71% and 81% yield respectively using 6,6-dimethyl-2-sulphonyloxomethylbicyclo[3.1.1] hept-2-ene (3).  All compounds were characterized by NMR, Infra-red, Micro Analysis and Mass Spectroscopy.</p>
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