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|a VanVeller, Brett
|e author
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|a Massachusetts Institute of Technology. Department of Chemistry
|e contributor
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|a Swager, Timothy M.
|e contributor
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|a Schipper, Derek James
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|a Vanveller, Brett
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|a Swager, Timothy Manning
|e contributor
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|a Swager, Timothy Manning
|e author
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|a Schipper, Derek James
|e author
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|a Polycyclic Aromatic Triptycenes: Oxygen Substitution Cyclization Strategies
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|b American Chemical Society,
|c 2013-04-04T17:32:24Z.
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|z Get fulltext
|u http://hdl.handle.net/1721.1/78290
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|a The cyclization and planarization of polycyclic aromatic hydrocarbons with concomitant oxygen substitution was achieved through acid catalyzed transetherification and oxygen-radical reactions. The triptycene scaffold enforces proximity of the alcohol and arene reacting partners and confers significant rigidity to the resulting π-system, expanding the tool set of iptycenes for materials applications.
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|a Natural Sciences and Engineering Research Council of Canada
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|a National Institutes of Health (U.S.) (NIH BRP grant R01 AG026240-01A1)
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|a Natural Sciences and Engineering Research Council of Canada (NSERC) (Postdoctoral Fellowship)
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|a United States. Air Force Office of Scientific Research (FA9550-10-1- 0395)
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|a en_US
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|a Article
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|t Journal of the American Chemical Society
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