with chloroform (three 100-ml portions). The extract was dried with sodium sulfate, the solvent was evaporated, and the residue was chromatographed in chloroform. The characteristics of X/fV and XXVII-XXIX are presented in Tables 345. 8,9;17,13,16-triazacvclooctadecane (XXVI) A 5.0-g (0.217 mole) s
Formation of dioxospiroindene[1,3]thiazine and thioxoindeno[2,1-d]imidazolone derivatives from alkenylidene-hydrazinecarbothioamides
✍ Scribed by Alaa A. Hassan; Ahmed M. Nour El-Din; Fathy F. Abdel-Latif; Sara M. Mostafa; Stefan Bräse
- Book ID
- 115063863
- Publisher
- Versita
- Year
- 2012
- Tongue
- English
- Weight
- 337 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0366-6352
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The reaction of (substituted) alkenylidene-hydrazinecarbothioamides with 2-(1,3-dioxo-2,3-dihydro-1H-inden-2-ylidene)propanedinitrile led to the formation of 1,3-dioxospiroindene[1,3]-thiazine and thioxoindeno[2,1-d]imidazolone derivatives in modest yields. In addition, 1,3-dihydroxyindan-2-ylidenepropanedinitrile was found. Explanations of these conversions involving nucleophilic reactions and condensations are presented.
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