Intermediates in the Hantzsch thiazole synthesis
RS Egan, J Tadanier, DL Garmaise…
Index: Egan,R.S. et al. Journal of Organic Chemistry, 1968 , vol. 33, # 12 p. 4422 - 4426
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Citation Number: 22
Abstract
The reaction of N-methyl-pdimethylaminothiobeneamide (3) with B number of a-halo ketones and one a-haloaldehyde gave stable Phydroxythiaaolinium salts (4) which could be subsequently dehydrated to the thiaaolium salts (5). When the intermediates were also substituted in the 5 position, both possible diastereoisomeric forms were detected by nmr spectroscopy. The effects of acidification and temperature variation on the nmr spectra ...
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[Garmaise,D.L. et al. Journal of Medicinal Chemistry, 1968 , vol. 11, # 6 p. 1205 - 1208]