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Reactions with 5-Substituted Isorhodanines. I (1972)

Kassab, N. A. L. ; Elnagdy, M. H. ; Messeha, N. A. ; [et al.]

New York, NY : Wiley-Blackwell

Journal für Praktische Chemie/Chemiker-Zeitung 314 (1972), S. 799-805

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ISSN: 0021-8383

Keywords: Chemistry ; Organic Chemistry

Source: Wiley InterScience Backfile Collection 1832-2000

Topics: Chemistry and Pharmacology

Notes: Treatment of 5-arylideneisorhodanines 1 with GRIGNARD reagents, effects addition of the reagent to the double bound of the lateral chain to yield products, proved to have structure 2.The thiono group in 1 and 2 condenses with aniline to yield the corresponding 5-substituted-4-phenylimino-2-thiazolidinones 3 and 4.Alkylation of 1 and 2 with alkyl halides or with ethereal diazomethane results in the formation of the S-alkyl derivatives 5 and 6, respectively.

Additional Material: 2 Tab.

Type of Medium: Electronic Resource

URL: http://dx.doi.org/10.1002/prac.19723140513

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