2026-09-20T23:48:03Zhttps://dspace.mit.edu/server/oai/requestoai:dspace.mit.edu:1721.1/785122022-01-13T07:53:58Zcom_1721.1_7582com_1721.1_7581col_1721.1_131024
Rick L. Danheiser.
Mamaliga, Galina
Massachusetts Institute of Technology. Department of Chemistry.
Massachusetts Institute of Technology. Department of Chemistry
2013-04-12T19:31:16Z
2013-04-12T19:31:16Z
2011
2012
http://hdl.handle.net/1721.1/78512
836812502
Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Chemistry, February 2012.
Cataloged from PDF version of thesis.
Includes bibliographical references.
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.
by Galina Mamaliga.
S.B.
69 p.
eng
Massachusetts Institute of Technology
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.
http://dspace.mit.edu/handle/1721.1/7582
Chemistry.
Progress towards the synthesis of tetracyclic heteroaromatic compounds via tandem benzannulation-cyclization strategies
Thesis
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Publication
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<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.</Abstract>
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