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- W2016765719 abstract "N -Benzoyl-2-oxa-3-azabicyclo[2.2.2]oct-5-ene undergoes cycloaddition with benzonitrile oxide affording a mixture of syn and anti regioisomeric cycloadducts. The anti cycloadducts were easily elaborated to stereodefined isoxazoline-carbocyclic aminols that served as synthons for the linear construction of pyrimidine nucleosides, while the syn cycloadducts do not enter the same synthetic route. N -Benzoyl-2-oxa-3-azabicyclo[2.2.2]oct-5-ene undergoes cycloaddition with benzonitrile oxide affording a mixture of syn and anti regioisomeric cycloadducts. The anti cycloadducts were easily elaborated to stereodefined isoxazoline-carbocyclic aminols that served as synthons for the linear construction of pyrimidine nucleosides, while the syn cycloadducts do not enter the same synthetic route." @default.
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- W2016765719 date "2008-07-01" @default.
- W2016765719 modified "2023-10-17" @default.
- W2016765719 title "From 1,3-cyclohexadiene through nitrosocarbonyl chemistry, the synthesis of pyrimidine isoxazoline-carbocyclic nucleosides" @default.
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- W2016765719 doi "https://doi.org/10.1016/j.tet.2008.05.061" @default.
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