105984-80-3Relevant academic research and scientific papers
NEW CHIRONS FOR THE SYNTHESIS OF FLUORINE-CONTAINING COMPOUNDS. AN EFFICIENT ENTRANCE TO α-MONO- AND POLY-FLUORO KETONES HAVING A CHIRAL α'-SULPHINYL SUBSTITUENT
Bravo, Pierfrancesco,Piovosi, Elena,Resnati, Giuseppe,Munari, Sergio De
, p. 115 - 122 (2007/10/02)
The lithium derivatives of optically pure alkyl p-tolyl sulphoxides, having both the R and S absolute configurations at the sulphur atom, have been condensed with the esters of mono- and poly-fluorocarboxylic acids to give several mono- and poly-fluoro ketones with a chiral sulphinyl substituent.The compounds having an alkyl residue on the α or α' position of the ketone group have also been obtained through alkylation of the di-, or mono-anion of the unsubstituted terms.Products chiral only at the sulphur atom, at the sulphur and the fluorinated carbon atom, or at the sulphur and the sulphinyl-substituted carbon have been obtained as single pure enantiomers.
Homochiral α-Fluoroketones from Racemic α-Fluorocarboxylic esters and Enantiomerically Pure Sulphoxides
Bravo, Pierfrancesco,Resnati, Giuseppe
, p. 218 - 219 (2007/10/02)
The α-fluoroalkyl ketones (3-7) carrying an alkyl, alkenyl, hydroxymethyl, or formyl residue were obtained in enantiomerically pure form by removing, by various methods, the auxiliary sulphinyl group from the α-fluoro α'-sulphinyl ketones (1) and (2) deri
