Results 61 to 70 of about 1,110,495 (128)
Organocatalytic Michael addition–lactonisation of carboxylic acids using α,β-unsaturated trichloromethyl ketones as α,β-unsaturated ester equivalents [PDF]
The authors thank the Royal Society for a University Research Fellowship (ADS), The Carnegie Trust for the Universities of Scotland (LCM), Syngenta/EPSRC (Case award to DGS), GSK/EPSRC (CASE award to SRS), the EU (IEF for CS), and the European Research ...
Morrill, L.C. +20 more
core +1 more source
Indium(III)‐Catalyzed Hydration and Hydroalkoxylation of α,β‐Unsaturated Ketones in Aqueous Media
The hydration of α,β-unsaturated ketones with water proceeded efficiently in the presence of In(OTf)3 (20 mol%) in aqueous media to afford synthetically versatile β-hydroxyketones in moderate to good yields with good functional group compatibility.
Chu, Xue-Qiang +11 more
core +1 more source
Iron-Catalyzed Chemoselective Reduction of α,β-Unsaturated Ketones
International audienceAn iron‐catalyzed chemo‐ and diastereoselective reduction of α,β‐unsaturated ketones into the corresponding saturated ketones in mild reaction conditions is reported herein.
Lator, Alexis +7 more
core +1 more source
Highly Enantioselective Transfer Hydrogenation of α,β-Unsaturated Ketones
We describe an efficient and highly enantioselective conjugate transfer hydrogenation of α,β-unsaturated ketones that is catalyzed by a salt made from tert-butyl valinate and a recently introduced powerful chiral phosphoric acid catalyst (TRIP)
Martin, N., List, B.
core +1 more source
Highly Enantioselective Transfer Hydrogenation of α,β-Unsaturated Ketones
We describe an efficient and highly enantioselective conjugate transfer hydrogenation of α,β-unsaturated ketones that is catalyzed by a salt made from tert-butyl valinate and a recently introduced powerful chiral phosphoric acid catalyst (TRIP)
Benjamin List (1505173) +1 more
core +1 more source
Efficient, selective: The primary amine salt 1 derived from quinine efficiently catalyzes the highly enantioselective hydroperoxidation of α,β‐unsaturated ketones furnishing stable and isolable cyclic peroxyhemiketals in enantiopure form. The versatility
List, B., Reisinger, C., Wang, X.
core +1 more source
A series of β-bromoketones and β-chloroketones were synthesized by the addition reactions of α,β-unsaturated ketones under BX3 (X = Br, Cl) and ethylene glycol reaction system.
Lee, Adam Shih-Yuan; Wang, Shu-Huei; Chang, Yu-Ting
core +1 more source
A reaction mixture of β,γ-unsaturated ketone and BF3·OEt2 in CH3OH was stirred at room temperature and β-methoxy ketone was produced in high yield. The β-amino ketone was obtained as the major product from a reaction mixture of β,γ-unsaturated ketone ...
Lee, Adam Shih-yuan; Wang, Shu-huei; Chang, Yu-ting; Chu, Shu-fang
core
A short and versatile synthesis of substituted quinolines is provided. Alkylation of sodium tolylsulfinate with bromomethyl- or chloromethyl ketones generates β-keto sulfones.
Henry Q. Zhang (2493607) +2 more
core +1 more source
An unusual oxidative palladium-catalyzed rearrangement of diaryl alkenyl carbinols to β,β-diaryl α,β-unsaturated ketones is described. The geometry of the alkene product is not determined by the electronic nature of the aryl substitutents but rather is ...
Arturo Orellana (1470739) +1 more
core +1 more source

