期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 87, 期 1, 页码 66-75出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.1c01863
关键词
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资金
- National Training Programs of Innovation and Entrepreneurship for Undergraduates [201810055095, 202010055079, 202110055069]
- Chemistry College of Nankai University
A four-component reaction strategy has been developed for access to acyclic nitrile-substituted all-carbon quaternary centers efficiently. By using DABCO-based ionic liquid catalyst, the reactions proceed smoothly under mild conditions, with water as the only byproduct. Some of the products exhibit excellent activity against specific fungi.
A four-component reaction strategy for access to acyclic nitrile-substituted all-carbon quaternary centers is disclosed. In the presence of a DABCO-based ionic liquid catalyst, the reactions proceed smoothly with a wide range of substrates efficiently to deliver nitrile-substituted all-carbon quaternary centers under mild reaction conditions. This protocol is further demonstrated as an efficient method for the construction of contiguous all-carbon quaternary centers. All the reactions are easily operated in a green manner, producing water as the only byproduct. Some of the products show excellent activity against specific fungi.
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