Effect of allylic substituents on the face selectivity of Diels-Alder reactions of semicyclic dienes

DOI: 10.1021/ja00179a036

Source and publish data:

Journal of the American Chemical Society p. 8472 - 8478 (1990)

Update date:2022-09-26

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Authors:

Datta Datta

Franck Franck

Tripathy

Quigley Quigley

Huang Huang

Chen Chen

Sihaed Sihaed

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Article abstract of DOI:10.1021/ja00179a036

Vinylcyclohexenes substituted allylically on the cyclohexene ring were examined as substrates in the Diels-Alder cycloaddition. In the octalin cycloaddition products, the relative stereochemistry of the one angular hydrogen relative to that of the allylic

Full text of DOI:10.1021/ja00179a036

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