Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5224952 | Tetrahedron | 2009 | 6 Pages |
Abstract
Polysubstituted 2H-pyran-2-ones and 5,6-dihydro-2H-pyran-2-ones were synthesized via the MCRs initiated by the hydroalkylation of alkynoates with activated methylenes. Under the optimized reaction conditions, the desired products were obtained in 47-88% isolated yields. The experimental results showed that the groups on activated methylenes act important roles in the nucleophilic attack fashion.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Wei-Bing Liu, Huan-Feng Jiang, Chun-Li Qiao,