Title of article
Sulfoxide-directed desymmetrisation of cyclohexa-1,4-dienes
Author/Authors
Elliott، نويسنده , , Mark C. and El Sayed، نويسنده , , Nahed Nasser Eid and Ooi، نويسنده , , Li-ling، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2007
Pages
4
From page
4561
To page
4564
Abstract
Cyclohexa-2,5-dien-1-ylmethanol derivatives have been subjected to a short sequence featuring esterification to introduce a malonate side-chain, oxidation of the doubly allylic position and stereoselective cyclisation. When used in conjunction with a chiral sulfoxide, the cyclisation is diastereoselective (2:1) favouring one of the diastereotopic double-bonds.
Journal title
Tetrahedron Letters
Serial Year
2007
Journal title
Tetrahedron Letters
Record number
1855364
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