期刊
CANADIAN JOURNAL OF CHEMISTRY
卷 92, 期 4, 页码 269-273出版社
CANADIAN SCIENCE PUBLISHING, NRC RESEARCH PRESS
DOI: 10.1139/cjc-2013-0435
关键词
indoles; TEMPO; biomimetic synthesis; trimerization
资金
- National Science Foundation of China [21162001, 21202023]
- National Key Technology R&D Program of China [2009BAI78B01]
- Jiangxi Province Key Support Program [2009BNB06200]
- Natural Science Foundation of Jiangxi Province [20132BAB203007]
- Jiangxi Province Office of Education Support Program [GJJ13666]
A simple, convenient, and efficient synthesis of 2-(1H-indol-3-yl)-2,3'-biindolin-3-one derivatives has been developed by the oxidative trimeric reaction of indoles using the TEMPO/CuCl2 catalyst system under ambient air. This methodology provides an alternative approach for the direct generation of all-carbon quaternary centers at the C-2 position of indoles.
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