Unusual gold(I)-catalyzed isomerization of 3-hydroxylated 1,5-enynes: Highly substrate-dependent reaction manifolds

Fabien Gagosz 1
1 DCSO - Laboratoire de synthèse organique
Abstract : (Chemical Equation Presented) The gold(I) isomerization of diversely substituted 3-hydroxylated enynes has led to the discovery of three new unreported skeletal rearrangements furnishing structures such as alkylidene-cyclopentenes, cyclohexadienes or a,ß-unsaturated aldehydes under very mild conditions. © 2005 American Chemical Society.
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Submitted on : Monday, March 24, 2014 - 4:56:08 PM
Last modification on : Thursday, February 7, 2019 - 5:16:35 PM

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Fabien Gagosz. Unusual gold(I)-catalyzed isomerization of 3-hydroxylated 1,5-enynes: Highly substrate-dependent reaction manifolds. Organic Letters, American Chemical Society, 2005, 7 (19), pp.4129-4132. ⟨10.1021/ol051397k⟩. ⟨hal-00954810⟩

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