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- W4240471624 endingPage "8585" @default.
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- W4240471624 abstract "The 1,3-dipolar cycloadditions of nitrones 1 and 2 to a series of 1,2-disubstituted electron-deficient olefins bearing an allylic stereocenter, 4−8, are reported. The syn/anti stereochemistry of the major endo adducts may be rationalized through the Houk transition-state model, but the possibility of intramolecular hydrogen bonding must be taken into account. In the case of the minor exo adducts the syn stereochemistry always predominates." @default.
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- W4240471624 date "1996-01-01" @default.
- W4240471624 modified "2023-10-17" @default.
- W4240471624 title "Diastereofacial Selectivity in the Cycloaddition of Nitrones to (<i>E</i>)-γ-Oxygenated α,β-Unsaturated Esters" @default.
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- W4240471624 doi "https://doi.org/10.1021/jo960960x" @default.
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