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ChemInform Abstract: 1,3-Thiazepines. Part 2. Reaction of 2-Iminohexahydrothiazepines with Phenyl Isocyanate and Isothiocyanates.

โœ Scribed by R. F. AMBARTSUMOVA; M. G. LEVKOVICH; N. D. ABDULLAEV


Publisher
John Wiley and Sons
Year
2010
Weight
30 KB
Volume
28
Category
Article
ISSN
0931-7597

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โœฆ Synopsis


1,3-Thiazepines. Part 2. Reaction of 2-Iminohexahydrothiazepines with Phenyl Isocyanate and Isothiocyanates.

-Reaction of the iminothiazepines (I) with phenyl isocyanate (II) gives the expected ureas (III) in good yields. In contrast, reaction with aryl isothiocyanates in refluxing toluene produces only substitution products (cf. (V)). Under more mild conditions (acetone, room temperature), unexpectedly substituted thioureas are obtained, e.g. compound (VII)/(VIII).


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ChemInform Abstract: 1,3-Thiazepines. Pa
โœ R. F. AMBARTSUMOVA; B. TASHKHODZHAEV; M. K. MAKHMUDOV ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 33 KB ๐Ÿ‘ 2 views

Part 4. Reaction of 2-Iminothiazepines with Methyl Acrylate. Crystal and Molecular Structure of 2-Phenylimino-3-(ฮฒ-methoxycarbonylethyl)-and 2-Benzyliminohexahydro-1,3thiazepines. -Reaction of 2-iminothiazepines (I) with methyl acrylate (II) proceeds at the endocyclic nitrogen to give the 2-imino-3