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Issue 5, 2001
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A novel oxime to pentathiepin cascade reaction

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Abstract

An extensive domino sequence, including a vinylogous sulfur-assisted Beckmann fragmentation, is involved in the one-pot conversion of a dioxime 3 by S2Cl2 into a cyanoethyl-1,2,3-dithiazole 5 and a novel tricyclic pentathiepin 6; the yield of 6 is increased by added lithium sulfide, and both 5 and 6 are formed in higher yield from 2-(cyanoethyl)cyclopentanone oxime 7; reaction mechanisms are proposed for these cascade reactions.

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Publication details

The article was received on 09 Jan 2001, accepted on 16 Jan 2001 and first published on 09 Feb 2001


Article type: Communication
DOI: 10.1039/B100366F
Citation: Chem. Commun., 2001,0, 403-404
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    A novel oxime to pentathiepin cascade reaction

    S. Macho, C. W. Rees, T. Rodríguez and T. Torroba, Chem. Commun., 2001, 0, 403
    DOI: 10.1039/B100366F

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