Synthesis of 6,6-disubstituted tetrahydrothiopheno [3,4-c] isoxazolines from β-nitroenones

Article abstract of DOI:10.1080/00397919708006787

β-Nitrosulfides 2, formed by Michael addition of prop-2-en-1-thiol to β-nitroenones 1 in the presence of a catalytic amount of triethylamine, undergo either Intramolecular Nitrile Oxide Cycloadditions (INOC) or Intramolecular Silylnitronate Cycloadditions

Full text of DOI:10.1080/00397919708006787

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Synthetic Communications: An
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Synthesis of 6,6-Disubstituted
Tetrahydrothiopheno [3,4-
c] Isoxazolines from β-
Nitroenones
Mohammed Ahrach a , Raphaël Schneider a , Philippe
Gérardin a & Bernard Loubinoux a
a LERMAB, Laboratoire de Chimie Organique-
Microbiologie , Université Henri Poincaré , Nancy-1,
Faculté des Sciences, BP 239, 54506, Vandoeuvre-
les-Nancy, France
Published online: 22 Aug 2006.
To cite this article: Mohammed Ahrach , Raphaël Schneider , Philippe Gérardin &
Bernard Loubinoux (1997) Synthesis of 6,6-Disubstituted Tetrahydrothiopheno [3,4-c]
Isoxazolines from β-Nitroenones, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 27:11, 1865-1876, DOI:
10.1080/00397919708006787
To link to this article: http://dx.doi.org/10.1080/00397919708006787
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