Diels-Alder Reaction of Dienes Having Stereogenic Allylic Substituents: Control of Diastereoface Selectivity by the Dienophile

DOI: 10.1021/ja00218a041

Source and publish data:

Journal of the American Chemical Society p. 3257 - 3262 (1988)

Update date:2022-08-04

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Authors:

Tripathy, R.

Franck, R. W.

Onan, K. D.

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Article abstract of DOI:10.1021/ja00218a041

The face selectivity of the Diels-Alder reaction of dienes having a stereogenic allylic carbon, as illustrated by structure 5, has been examined.Whereas N-phenylmaleimide and maleic acid afforded adducts resulting from like topicity, tetracyanoethylene an

Full text of DOI:10.1021/ja00218a041

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