Author:
Török Marcel,Dzurilla Milan,Kutschy Peter,Imrich Ján,Danihel Ivan,Rademacher Paul,Bandmann Heinz
Abstract
The N-(4-substituted phenyl)-N'-cyclohexylideneacetylthioureas IIa - IIf were readily prepared by the reaction of cyclohexylideneacetyl isothiocyanate I with 4-substituted anilines. They were cyclized to the 2-(4-substituted phenylimino)-4-oxo-1,3-thiazaspiro[5.5]undecanes IIIa - IIIe in the presence of boron trifluoride etherate and to the 1-(4-substituted phenyl)-4-oxo-2-thioxo-1,3-diazaspiro[5.5]undecanes IVa, IVc - IVf in alkaline medium.
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
4 articles.
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