A mild, one-pot procedure to produce 3-substituted allylic alcohols from α,β-unsaturated ketones is described. The addition of an organolithium nucleophile produces a tertiary allylic alcohol as an intermediate, which undergoes a 1,3-OH-migration assisted by FeCl 2 . The proposed mechanism indicates that a syn -facial migration occurs for the major product. Yields as high as 98% for the one-pot reaction are reported.

Eastern hemlock (Tsuga canadensis (L.) Carrière) is an eastern North American conifer threatened by the invasive hemlock woolly adelgid (Adelges tsugae Annand). Changes in foliar terpenes and phenolics were evaluated in new (current-year growth) and mature (1-year-old growth) hemlock needles during the growing season and into plant dormancy. From April through September, foliar concentrations of nonvolatile soluble phenolics, condensed tannins, lignin, mono- and sesquiterpenes, α-pinene, camphene, isobornyl acetate, and diterpene resin were quantified. After September, additional analyses of metabolites that continued to differ significantly between new and mature foliage were carried out. Total soluble phenolic and condensed tannin concentrations in new foliage remained low relative to those of mature foliage throughout the growing season and converged in December. Lignin concentration in new foliage converged with that of mature foliage by July. Concentrations of α-pinene, camphene, isobornyl acetate, and diterpene resin in new foliage converged with those of mature foliage within 1 month of budbreak. The convergence of terpene concentrations in new and mature foliage suggests that these metabolites may play a role in herbivore defense during the peak growing season. Conversely, soluble phenolics, including condensed tannins, may defend foliage from herbivory outside of the spring growth period.