Abstract
The intramolecular Diets-Alder reactions of a series of ether-tethered trienes 3a-3o show varying selectivities according to the nature of the dienophile-activating group and the presence of substituents in the linking chain. Some tether-cleaving reactions are reported.
| Original language | English |
|---|---|
| Pages (from-to) | 695-724 |
| Number of pages | 30 |
| Journal | Tetrahedron |
| Volume | 52 |
| Issue number | 2 |
| Publication status | Published - 8 Jan 1996 |
Keywords
- SILYL ACETAL TRIENES
- STEREOCHEMICAL ASPECTS
- LEWIS ACID
- CYCLOADDITIONS
- CLEAVAGE
- STEREOCONTROL
- ALLYLSILANES
- CHEMISTRY
- EFFICIENT
- STRATEGY
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