Abstract
Four substituted cis and trans-4,5-dihydroxyhexahydropyridazines that were expected to undergo pH induced conformational switching were synthesized and carefully investigated by NMR analyses and calculations. For two of the compounds a large difference in pKa existed between the two possible chair conformers and for one compound this resulted in conformational switching as a result of pH change. For the first time it is shown that the pKa directly reflects the conformational equilibrium of conformers.
Original language | English |
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Journal | Organic & Biomolecular Chemistry |
Volume | 13 |
Issue number | 10 |
Pages (from-to) | 3116-3121 |
Number of pages | 6 |
ISSN | 1477-0520 |
DOIs | |
Publication status | Published - 14 Mar 2015 |