Micellar effects on the regiochemistry of a Diels-Alder reaction

DOI: 10.1016/S0040-4039(00)79003-4

Source and publish data:

Tetrahedron Letters p. 6415 - 6418 (1992)

Update date:2022-08-04

Topics:

Authors:

Jaeger, David A.

Wang, Jinkang

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Article abstract of DOI:10.1016/S0040-4039(00)79003-4

The Diels-Alder reaction of surfactant 1,3-diene 1 and surfactant dienophile 2 under aqueous micellar conditions gave up to a 3.0:1 ratio of cycloadducts 11 and 12. The regioselectivity of the reaction was controlled by the alignment of reactants at the m

Full text of DOI:10.1016/S0040-4039(00)79003-4

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