Abstract
A stereoselective construction of cis- and trans-2,6-disubstituted tetrahydropyranones, based on strategy which combines an asymmetric alkylation and ring closing metathesis for the formation of a cyclic enol ether, is reported.
Original language | English |
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Pages (from-to) | 179-183 |
Number of pages | 5 |
Journal | Heterocycles |
Volume | 62 |
State | Published - 1 Jan 2004 |