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• W2079854443 abstract "Intermolecular Michael-type conjugate additions of some in situ-generated ring-substituted nitrosocyclohexenes with both carbon- and heteronucleophiles have been found to be highly stereoselective, leading predominantly (or exclusively) to products resulting from axial attack on a half-chair conformation of the nitrosoalkene substrate." @default.
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• W2079854443 date "2011-10-01" @default.
• W2079854443 modified "2023-10-03" @default.
• W2079854443 title "Stereochemical investigation of conjugate additions of carbon- and heteronucleophiles to ring-substituted nitrosocyclohexenes" @default.
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• W2079854443 doi "https://doi.org/10.1016/j.tet.2011.08.054" @default.
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