664343-08-2Relevant articles and documents
Diastereoselectivity in the Carroll rearrangement of β-keto esters of tertiary allylic alcohols
Jung, Michael E.,Duclos, Brian A.
, p. 107 - 109 (2007/10/03)
Carroll rearrangement of β-keto esters derived from tertiary allylic alcohols, for example, 7, under basic conditions followed by decarboxylation of the resulting β-keto acids yielded the expected γ, δ-unsaturated methyl ketones 8 with a range of olefin geometries from 100:0 to 1:1.8 E/Z, depending on the relative steric requirements of the two groups at the allylic center.