Journal of Organic Chemistry p. 1859 - 1874 (1993)
Update date:2022-07-30
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Denmark, Scott E.
Schnute, Mark E.
Senanayake, C. B. W.
The stereochemical course of the tandem <4+2>/<3+2> nitroalkene cycloaddition with chiral enol ethers has been shown to exhibit remarkable sensitivity to the nature of the Lewis acid promoter.Cycloadditions using (+)-camphor-derived vinyl ether 3 or (-)-t
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