Abstract
A new method for the synthesis of 2,3-dihydrofurans from readily available starting enones and α-nitro carbonyl compounds has been developed. This protocol can provide a novel and effective methodology for the preparation of 2,3-dihydrofurans in a stereoselective fashion. With 1,4-dien-3-ones, 2,3-dihydrofurans and cyclohexenecarboxylates were produced and high chemoselectivity was observed in different solvents.
Original language | English |
---|---|
Pages (from-to) | 7511-7516 |
Number of pages | 6 |
Journal | Tetrahedron |
Volume | 64 |
Issue number | 32 |
DOIs | |
Publication status | Published - 2008 Aug 4 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry