97181-65-2Relevant academic research and scientific papers
REDUCTION DES ANHYDRIDES BICYCLIQUES CONDENSES PAR LE BROMURE DE CYCLOPENTYLMAGNESIUM
Canonne, P.,Akssira, M.
, p. 1297 - 1300 (2007/10/02)
Greatly different product distributions were observed in the reactions of cyclopentyl- and isopropylmagnesium bromides with cyclohexane-, cyclohex-4-ene- and cyclobutane-1,2 dicarboxylic anhydrides.Cyclopentylmagnesium bromide yielded reduction products with high stereoselectivity whereas the isopropylmagnesium bromide provided the corresponding trans diastereomeric ketoacids via an addition enolization process.
Syntheses stereoselectives des γ-lactones bicycliques condensees
Canonne, P.,Akssira, M.
, p. 3695 - 3704 (2007/10/02)
A highly stereoselective synthesis of trans/trans and cis/trans bicyclic γ-lactones is described using bicyclic dicarboxylic anhydrides.
