Asymmetric Diels-Alder reactions of enantiopure 1-methoxy-3-(phenyl-2- hydroxyethylsulfinyl)-1,3-butadienes

DOI: 10.1016/S0957-4166(00)86232-1

Source and publish data:

Tetrahedron Asymmetry p. 805 - 808 (1994)

Update date:2022-08-03

Topics: Enantiopure Asymmetric Diels-Alder Reactions

Authors:

Aversa Aversa

Bonaccorsi

Giannetto

Jones Jones

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Article abstract of DOI:10.1016/S0957-4166(00)86232-1

Enantiopure 1-methoxy-3-(1-phenyl- and 2-phenyl-2-hydroxyethylsulfinyl)- 1,3-butadienes were prepared from ethyl mandelate. Diels-Alder reactions with methyl acrylate proceeded with complete regioselectivity and high diastereoselectivity.

Full text of DOI:10.1016/S0957-4166(00)86232-1

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