An alternative enantioselective synthesis of (+)-tricyclodecadienone

DOI: 10.1016/S0040-4039(97)00392-4

Source and publish data:

Tetrahedron Letters p. 2527 - 2530 (1997)

Update date:2022-08-29

Topics:

Authors:

Knol, Joop

Feringa, Ben L.

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Article abstract of DOI:10.1016/S0040-4039(97)00392-4

The enantiomerically pure endo-cycloadduct 2 obtained from the thermal Diels-Alder reaction of 5R-(l-menthyloxy)-2(5H)-furanone with cyclopentadiene is converted into (+)-tricyclo[5.2.1.0^2.6]decadi-4,8-en-3one ((+)-1) in a one-pot procedure via

Full text of DOI:10.1016/S0040-4039(97)00392-4

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