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- W1972476073 abstract "Reaction of acryloyl chloride with dienamines derived from 3-alkyl-5,5-dimethylcyclohex-2-enones gives mainly the corresponding 6-alkyl-8,8-dimethylbicyclo[3,3,1]non-6-ene-2,9-diones formed by initial carbon–carbon bond formation at the β-position (C-2) and cyclisation at C-6. A tricyclic compound formed by reaction at the β-and δ-positions was also isolated in one case, but in very low yield. Reaction of acryloyl chloride with acyclic linear and cross-conjugated dienamines gives mainly the corresponding 2-alkyl-4-alkenyl- and 2-alkenyl-4-alkyl-3-morpholinocyclohex-2-enones respectively." @default.
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- W1972476073 date "1970-01-01" @default.
- W1972476073 modified "2023-09-24" @default.
- W1972476073 title "Enamine chemistry. Part VIII. Reaction of acryloyl chloride with dienamines" @default.
- W1972476073 doi "https://doi.org/10.1039/j39700001477" @default.
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