Abstract
Iodolactonisations of (Z)- or (E)-3-silyloxy-5-alkenoic acids [1 and 7] both lead to transdisubstituted valerolactones [6 and 8], which differ only in the stereochemistry of the iodine substituent.
| Original language | English |
|---|---|
| Pages (from-to) | 6505-6506 |
| Number of pages | 2 |
| Journal | Tetrahedron Letters |
| Volume | 33 |
| Issue number | 43 |
| DOIs | |
| Publication status | Published - 1992 |
Keywords
- methyl groups
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