Functionalized carbocyclic rings via intramolecular Diels-Alder reactions of in situ-generated, γ substituted, heteroatom-stabilized allyl cations in acidic polar media

DOI: 10.1016/S0040-4039(98)02637-9

Source and publish data:

Tetrahedron Letters p. 1265 - 1268 (1999)

Update date:2022-07-29

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Authors:

Grieco, Paul A.

Kaufman, Michael D.

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Article abstract of DOI:10.1016/S0040-4039(98)02637-9

The synthesis of highly structured carbocyclic ring systems possessing quaternary carbon atoms has been realized via intramolecular Diels-Alder reactions of in situ-generated, γ substituted, heteroatom-stabilized allyl cations in acidic polar media.

Full text of DOI:10.1016/S0040-4039(98)02637-9

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