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Gold‐Catalyzed Enantioselective Synthesis,Crystal Structure,and Photophysical/Chiroptical Properties of Aza[10]helicenes
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
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/
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.
Keywords:alkynes  asymmetric catalysis  azahelicenes  gold  hydroarylation
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