Abstract
The hydrochlorides of 27 Michael adducts, formed from alkylthiols and chalcones mono-substituted successively in each ring by nitro, chloro, and methoxy groups, were thermally cleaved by hot water. The amount of cleavage was readily determined iodimetrically.
Cite
CITATION STYLE
APA
Allen, C. F. H., Fournier, J. O., & Humphlett, W. J. (1964). THE THERMAL REVERSIBILITY OF THE MICHAEL REACTION: IV. THIOL ADDUCTS. Canadian Journal of Chemistry, 42(11), 2616–2620. https://doi.org/10.1139/v64-383
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