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박영석

Park, Young S.
Advanced Organic Materials Lab.
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An Aza-Diels-Alder Approach to Crowded Benzoquinolines

Author(s)
Mazaheripour, AmirDibble, David J.Umerani, Mehran J.Park, Young S.Lopez, RobertLaidlaw, DylanVargas, EribertoZiller, Joseph W.Gorodetsky, Alon A.
Issued Date
2016-01
DOI
10.1021/acs.orglett.5b02939
URI
https://scholarworks.unist.ac.kr/handle/201301/20039
Fulltext
http://pubs.acs.org/doi/abs/10.1021/acs.orglett.5b02939
Citation
ORGANIC LETTERS, v.18, no.2, pp.156 - 159
Abstract
Graphene nanoribbons (GNRs) are promising candidate materials for the next generation of nanoscale electronics. Described herein is the synthesis of 2,4,6-substituted benzoquinolines, which constitute building blocks for nitrogen-doped GNRs. The presented facile and modular aza-Diels-Alder chemistry accommodates the installation of diverse functionalities at the crowded benzoquinolines 2 positions. Given the general utility of the benzoquinoline motif, these findings hold relevance not only for carbon-based electronics but also for a range of chemical disciplines
Publisher
AMER CHEMICAL SOC
ISSN
1523-7060
Keyword
PROCESSABLE GRAPHENE NANORIBBONSBOTTOM-UP SYNTHESISNANOGRAPHENEDERIVATIVESCHEMISTRYQUINOLINESHEETS

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