A new benzannulation reaction

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dc.contributor.advisorCiufolini, Marco A.en_US
dc.creatorWeiss, Trent Jasonen_US
dc.date.accessioned2009-06-04T00:14:10Zen_US
dc.date.available2009-06-04T00:14:10Zen_US
dc.date.issued1994en_US
dc.description.abstractA new benzannulation reaction was discovered. The reaction involves intramolecular attack into a carbon-carbon triple-bond by the alpha position of a beta-ketoester under acidic conditions. Four different beta-ketoester starting materials were prepared and were successfully cyclized. This benzannulation methodology should provide a convenient pathway for forming aromatic products to be used as building blocks in the syntheses of anti-tumor antibiotics.en_US
dc.format.extent95 p.en_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.callnoTHESIS CHEM. 1994 WEISSen_US
dc.identifier.citationWeiss, Trent Jason. "A new benzannulation reaction." (1994) Master’s Thesis, Rice University. <a href="https://hdl.handle.net/1911/13913">https://hdl.handle.net/1911/13913</a>.en_US
dc.identifier.urihttps://hdl.handle.net/1911/13913en_US
dc.language.isoengen_US
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.en_US
dc.subjectOrganic chemistryen_US
dc.titleA new benzannulation reactionen_US
dc.typeThesisen_US
dc.type.materialTexten_US
thesis.degree.departmentChemistryen_US
thesis.degree.disciplineNatural Sciencesen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelMastersen_US
thesis.degree.nameMaster of Artsen_US
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