Gold‐Catalyzed Enantioselective Synthesis,Crystal Structure,and Photophysical/Chiroptical Properties of Aza[10]helicenes |
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Authors: | Maya Tanaka Dr Yu Shibata Kyosuke Nakamura Kota Teraoka Prof?Dr Hidehiro Uekusa Dr Kazuko Nakazono Prof?Dr Toshikazu Takata Prof?Dr Ken Tanaka |
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Institution: | 1. Department of Applied Chemistry, Graduate School of Science and Engineering, Tokyo Institute of Technology, Tokyo, Japan;2. Department of Applied Chemistry, Graduate School of Engineering, Tokyo University of Agriculture and Technology, Tokyo, Japan;3. Department of Chemistry and Materials Science, Graduate School of Science and Engineering, Tokyo Institute of Technology, Tokyo, Japan;4. Department of Organic and Polymeric Materials, Graduate School of Science and Engineering, Tokyo Institute of Technology, Tokyo, Japan;5. http://www.apc.titech.ac.jp/~ktanaka/ |
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Abstract: | The enantioselective synthesis of an aza10]helicene, possessing two pyridone units, has been achieved by the gold‐catalyzed intramolecular quadruple hydroarylation of a tetrayne. This aza10]helicene was successfully converted into a fully aromatic aza10]helicene, possessing two pyridine units. Structure–photophysical and chiroptical properties relationship in a series of azahelicene isomers has also been disclosed. |
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Keywords: | alkynes asymmetric catalysis azahelicenes gold hydroarylation |
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