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            <mods:title>Twofold Heck / 6π-Electrocyclization and Regioselective Palladium(0)-Catalyzed Reactions of Brominated Thiophenes, Pyrroles, Imidazoles and Indoles</mods:title>
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            <mods:namePart type="termsOfAddress">Prof. Dr. Dr. h. c.</mods:namePart>
            <mods:namePart type="given">Peter</mods:namePart>
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            <mods:namePart type="termsOfAddress">Prof. Dr.</mods:namePart>
            <mods:namePart type="given">Jens</mods:namePart>
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            <mods:namePart>Universität Rostock</mods:namePart>
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          <mods:identifier type="doi">10.18453/rosdok_id00000988</mods:identifier>
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            <mods:publisher>Universität Rostock</mods:publisher>
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            <mods:dateIssued encoding="w3cdtf" keyDate="yes">2011</mods:dateIssued>
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          <mods:abstract type="summary" xml:lang="en" xlink:type="simple">This thesis presents site-selective Suzuki-Miyaura reactions of 2,3,5-tribromo-thiophene, 2,4,5-tribromothiophene and 2,3,5-tribromo-N-methylpyrrole, which are controlled by steric and electronic parameters. Palladium-catalyzed Heck reactions of brominated thiophenes, N-methylimidazole, N-methylpyrrole and N-methylindole are also presented. The products were transformed by subsequent 6π-electrocyclization and dehydrogenation to functionalized benzothiophenes, dibenzothiophenes, benzimidazoles, indoles and carbazoles, respectively.</mods:abstract>
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            <mods:topic>palladium</mods:topic>
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          <mods:subject authority="author" xlink:type="simple">
            <mods:topic>Suzuki reaction</mods:topic>
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          <mods:subject authority="author" xlink:type="simple">
            <mods:topic>Heck reaction</mods:topic>
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          <mods:subject authority="author" xlink:type="simple">
            <mods:topic>electrocyclizations</mods:topic>
          </mods:subject>
          <mods:subject authority="author" xlink:type="simple">
            <mods:topic>heterocycles</mods:topic>
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