Abstract
<div class="line" id="line-5"> Differentially substituted bridged pyridinium oximes are necessary in research on antidotes for organophosphate poisoning. A solid‐phase synthesis would improve the yield and ease of purification of these compounds. To predict the lability of the linker in the final step of our proposed synthesis, we synthesized a series of pyridine and <i> N </i> ‐methyl pyridinium acetals. These compounds proved to be resistant to acid catalyzed hydrolysis. This stability may be useful for synthetic manipulation of pyridine aldehydes.</div>
Original language | American English |
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Journal | Journal of Heterocyclic Chemistry |
Volume | 40 |
DOIs | |
State | Published - Mar 2009 |
Disciplines
- Chemistry