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 |
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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