Progress towards the synthesis of tetracyclic heteroaromatic compounds via tandem benzannulation-cyclization strategies
Name
836812502-MIT.pdf
Description
Full printable version
Size
4.19 MB
Format
Adobe PDF
Checksum (MD5)
71682710576100d9f427a5793aef0eac
Author(s)
Mamaliga, Galina
Advisor(s)
Rick L. Danheiser.
Date Issued
2012
Publisher
Massachusetts Institute of Technology
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.
Description
Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Chemistry, February 2012.
Cataloged from PDF version of thesis.
Includes bibliographical references.
Subjects
Chemistry.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
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copyright. They may be viewed from this source for any purpose, but
reproduction or distribution in any format is prohibited without written
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