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- W2084382308 abstract "Monomeric selenoketones (selones) have been prepared from di-t-butyl ketone and (–)-1,3,3-trimethylnorbornan-2-one through heating their triphenylphosphoranylidenehydrazones with selenium. Although selones show greater reactivity towards diazo-compounds than thiones it was still not possible to prepare the elusive tetra-t-butylethylene. However, (–)-1,1′,3,3,3′,3′-hexamethyl-2,2′-binorbornylidene, which is a ‘tied back’ tetra-t-butylethylene, was obtained without difficulty and is stable to oxygen." @default.
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- W2084382308 date "1976-01-01" @default.
- W2084382308 modified "2023-10-16" @default.
- W2084382308 title "Olefin synthesis by two-fold extrusion processes. Part 3. Synthesis and properties of hindered selenoketones (selones)" @default.
- W2084382308 doi "https://doi.org/10.1039/p19760002079" @default.
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