946485-84-3Relevant academic research and scientific papers
Lewis base activation of Lewis acids: Catalytic, enantioselective vinylogous aldol addition reactions
Denmark, Scott E.,Heemstra Jr., John R.
, p. 5668 - 5688 (2008/02/10)
(Chemical Equation Presented) The generality of Lewis base catalyzed, Lewis acid mediated, enantioselective vinylogous aldol addition reactions has been investigated. The combination of silicon tetrachloride and chiral phosphoramides is a competent catalyst for highly selective additions of a variety of α,β-unsaturated ketone-, 1,3-diketone-, and α,β- unsaturated amide-derived dienolates to aldehydes. These reactions provided high levels of γ-site selectivity for a variety of substitution patterns on the dienyl unit. Both ketone- and morpholine amide-derived dienol ethers afforded high enantio- and diastereoselectivity in the addition to conjugated aldehydes. Although α,β-unsaturated ketone-derived dienolate did not react with aliphatic aldehydes, α,β-unsaturated amide-derived dienolates underwent addition at reasonable rates affording high yields of vinylogous aldol product. The enantioselectivities achieved with the morpholine derived-dienolate in the addition to aliphatic aldehydes was the highest afforded to date with the silicon tetrachloride-chiral phosphoramide system. Furthermore, the ability to cleanly convert the morpholine amide to a methyl ketone was demonstrated.
Lewis base activation of Lewis acids: Vinylogous aldol additions of silyl dienol ethers to aldehydes
Denmark, Scott E.,Heemstra Jr., John R.
, p. 2411 - 2416 (2007/10/03)
Highly regioselective vinylogous aldol additions of silyl dienol ethers derived from simple α,β-unsaturated ketones are described. The catalyst system of silicon tetrachloride activated by chiral bisphosphoramide (R,R)-1 effectively promotes the addition
