4.8 Article

An Aza-Diels-Alder Approach to Crowded Benzoquinolines

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ORGANIC LETTERS
卷 18, 期 2, 页码 156-159

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b02939

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  1. Office of Naval Research [N000141210491, N000141310650, N000141512680]
  2. NSF [CHE-0840513]
  3. U.S. Department of Defense (DOD) [N000141512680] Funding Source: U.S. Department of Defense (DOD)

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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.

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