Effect of Catalyst and Solvent on the Stereochemistry of Diels-Alder Reactions Between Cyclopentadiene and 3-Phenylsulfinylprop-2-enoic Acids and Methyl Esters

DOI: 10.1071/CH9841677

Source and publish data:

Australian Journal of Chemistry p. 1677 - 1688 (1984)

Update date:2022-08-02

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Authors:

Proust, Simone M.

Ridley, Damon M.

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Article abstract of DOI:10.1071/CH9841677

In Diels-Alder reactions between cyclopentadiene and the isomeric 3-phenylsulfinylprop-2-enoic acids and methyl esters, greatest stereoselectivity (94percent d.e.) results when methyl (Z)-3-phenylsulfinylprop-2-enoate (7) and benzene solvent are used.The

Full text of DOI:10.1071/CH9841677

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