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Progress towards the synthesis of tetracyclic heteroaromatic compounds via tandem benzannulation-cyclization strategies

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dc.contributor.advisor Rick L. Danheiser. en_US
dc.contributor.author Mamaliga, Galina en_US
dc.contributor.other Massachusetts Institute of Technology. Department of Chemistry. en_US
dc.date.accessioned 2013-04-12T19:31:16Z
dc.date.available 2013-04-12T19:31:16Z
dc.date.copyright 2011 en_US
dc.date.issued 2012 en_US
dc.identifier.uri http://hdl.handle.net/1721.1/78512
dc.description Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Chemistry, February 2012. en_US
dc.description Cataloged from PDF version of thesis. en_US
dc.description Includes bibliographical references. en_US
dc.description.abstract A tandem benzannulation-cyclization strategy was successfully applied to the synthesis of a tetracyclic heteroaromatic compound expected to have interesting electronic properties. Benzannulation of a diazo ketone and a ynamide yielded a highly substituted aniline that was cyclized to indole according to protocols developed in our laboratory previously. en_US
dc.description.statementofresponsibility by Galina Mamaliga. en_US
dc.format.extent 69 p. en_US
dc.language.iso eng en_US
dc.publisher Massachusetts Institute of Technology en_US
dc.rights M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. en_US
dc.rights.uri http://dspace.mit.edu/handle/1721.1/7582 en_US
dc.subject Chemistry. en_US
dc.title Progress towards the synthesis of tetracyclic heteroaromatic compounds via tandem benzannulation-cyclization strategies en_US
dc.type Thesis en_US
dc.description.degree S.B. en_US
dc.contributor.department Massachusetts Institute of Technology. Department of Chemistry. en_US
dc.identifier.oclc 836812502 en_US


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