期刊
ORGANIC LETTERS
卷 22, 期 1, 页码 102-105出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b04015
关键词
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资金
- National Natural Science Foundation of China [21602207]
- Foundation of Henan Educational Committee [17A150022]
- Doctoral Research Fund of Zhengzhou University of Light Industry [2014BSJJ009]
Alkynol served as an enolizable carbonyl equivalent to react with (thio)urea and aromatic aldehydes, furnishing a variety of spirofuran-hydropyrimidinone compounds in good yields and excellent diastereoselectivities. The one-pot multi-component reactions were realized with co-catalysis of palladium chloride and trifluoroacetic acid through a Biginelli-like tandem reaction pathway.
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