Tandem Inter /Intra Nitroalkene Cycloadditions. 5. Origin of the Lewis Acid Dependent Reversal of Stereoselektivity

DOI: 10.1021/jo00059a044

Source and publish data:

Journal of Organic Chemistry p. 1859 - 1874 (1993)

Update date:2022-07-30

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Authors:

Denmark, Scott E.

Schnute, Mark E.

Senanayake, C. B. W.

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Article abstract of DOI:10.1021/jo00059a044

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

Full text of DOI:10.1021/jo00059a044

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