Abstract
Nuclear Overhauser enhancement experiments show that migratory attitudes of alkyl groups in various vic-dihydroxybacteriopurpurins are different for individual stereoisomers. Long wavelength absorption maxima of ketobacteriopurpurins obtained from pinacol-pinacolone rearrangements of the corresponding diols are influenced by the position of the keto group in the macrocycle; differences in these maxima are diminished by introduction of electron-withdrawing substituents.
| Original language | English |
|---|---|
| Pages (from-to) | 747-750 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 37 |
| Issue number | 6 |
| DOIs | |
| State | Published - Feb 5 1996 |
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