Abstract
Homo- and cross-couplings of vinylketene silyl acetals were found to be effectively promoted by titanium tetrachloride to give the corresponding unsaturated diesters in good yields. The reactions between two different ketene silyl acetate afforded the corresponding cross-coupling products in unexpectedly good selectivities.
| Original language | English |
|---|---|
| Pages (from-to) | 785-788 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 24 |
| Issue number | 8 |
| DOIs | |
| State | Published - 1983 |
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