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- W2952213019 abstract "Cycloaddition of nitrones to diethyl arylmethylene malonates occurred with very high selectivity to furnish 3,5-trans-2,3,5-triaryl-4,4-dicarbethoxy isoxazolidines. This is in contrast with the nitrone cycloadditions to other α,β-conjugated carbonyl derivatives where two diastereoisomeric (and on occasion regioisomeric) cycloadducts are generally obtained." @default.
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- W2952213019 date "2007-09-01" @default.
- W2952213019 modified "2023-09-23" @default.
- W2952213019 title "1,3-Dipolar cycloadditions: part XIV – Highly selective cycloadditions of C, N-diaryl nitrones to diethyl aryl methylene malonates¹" @default.
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