<?xml version="1.0"?>
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">Synthesis of functionalized homophthalates, salicylates, diaryl ethers and dihydroisocoumarins based on cyclocondensation reactions of 1,3-dicarbonyl compounds and 1,3-bis(silyloxy)-1,3-butadienes</dc:title>
  <dc:contributor xmlns:dc="http://purl.org/dc/elements/1.1/">Sher, Muhammad , 1977-</dc:contributor>
  <dc:type xmlns:dc="http://purl.org/dc/elements/1.1/">Text</dc:type>
  <dc:type xmlns:dc="http://purl.org/dc/elements/1.1/">theses</dc:type>
  <dc:type xmlns:dc="http://purl.org/dc/elements/1.1/">Text</dc:type>
  <dc:type xmlns:dc="http://purl.org/dc/elements/1.1/">Hochschulschrift</dc:type>
  <dc:date xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">2008</dc:date>
  <dc:date xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">2008</dc:date>
  <dc:language xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">eng</dc:language>
  <dc:format xmlns:dc="http://purl.org/dc/elements/1.1/">electronic resource</dc:format><dc:format xmlns:dc="http://purl.org/dc/elements/1.1/">remote</dc:format><dc:format xmlns:dc="http://purl.org/dc/elements/1.1/">Computermedien</dc:format><dc:format xmlns:dc="http://purl.org/dc/elements/1.1/">Online-Ressource</dc:format><dc:format xmlns:dc="http://purl.org/dc/elements/1.1/">Online-Ressource graph. Darst.</dc:format>
  <dc:description xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">Regioselective cyclocondensation reactions of 1,3-bis(silyl enol ethers) with different mono(silyl enol ethers) provide an elegant approach for the synthesis of various complex carba- and heterocycles from simple starting materials. Salicylates, diarylethers, resorcins and 3-aryl-3,4-dihydroisocoumarins are prepared based on regioselective [3+3] cyclocondensation reactions of 1,3-bis(silyl enol ethers) with 1,1,3,3-tetramethoxypropane, 2-aryloxy-3-(silyloxy)alk-2-en-1-ones, 3,3-dimethoxypentanoyl chloride and 1-hydroxy-5-silyloxy-4-en-3-ones respectively. In addition, 4,5-diaryl-1,2,3-benzenetricarboxylates are prepared by reaction of 4-hydroxycyclopent-2-en-1-one-2-carboxylates with dimethyl acetylenedicarboxylate. In addition, 1-(2,2-dimethoxyethyl)-1,2,3-triazoles are prepared by regioselective copper(I)-catalyzed [3+2] cyclization of 2-azido-2,2-dimethoxyethane with alkynes.</dc:description>
  <dc:description xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">Muhammad Sher</dc:description>
  <dc:description xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">Rostock, Univ., Mathematisch-Naturwiss. Fak., Diss., 2008</dc:description>
  <dc:subject xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">540</dc:subject>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2008-0105-5</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">http://rosdok.uni-rostock.de/resolve?urn=urn:nbn:de:gbv:28-diss2008-0105-5&amp;pdf</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">http://nbn-resolving.de/urn:nbn:de:gbv:28-diss2008-0105-5</dc:identifier>
  <dc:relation xmlns:dc="http://purl.org/dc/elements/1.1/">Synthesis of functionalized homophthalates, salicylates, diaryl ethers and dihydroisocoumarins based on cyclocondensation reactions of 1,3-dicarbonyl compounds and 1,3-bis(silyloxy)-1,3-butadienes--(DE-627)584683723</dc:relation>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">urn:nbn:de:gbv:28-diss2008-0105-5</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:srw_dc="info:srw/schema/1/dc-schema">oclc: 301999217</dc:identifier>
  <dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">ppn:
				(DE-627)587371811</dc:identifier>
</oai_dc:dc>
