An efficient approach to either enantiomer of trans-cyclohex-2-ene-1,4-diol

Graphic (1 S,4 S)-Cyclohex-2-ene-1,4-diol has been synthesised starting from a chiral p-benzoquinone equivalent. The sequence can be equally applied to the preparation of the (1 R,4 R)-enantiomer of the target diol.

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Bibliographic Details
Published in:Tetrahedron: asymmetry 2004-04, Vol.15 (7), p.1151-1155
Main Authors: Alibés, Ramon, de March, Pedro, Figueredo, Marta, Font, Josep, Marjanet, Georgina
Format: Article
Language:English
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Summary:Graphic (1 S,4 S)-Cyclohex-2-ene-1,4-diol has been synthesised starting from a chiral p-benzoquinone equivalent. The sequence can be equally applied to the preparation of the (1 R,4 R)-enantiomer of the target diol.
ISSN:0957-4166
1362-511X
DOI:10.1016/j.tetasy.2004.02.003