77291-90-8Relevant articles and documents
Enantioselective preparation of 2,4-disubstituted azetidines
Marinetti, Angela,Hubert, Philippe,Genêt, Jean-Pierre
, p. 1815 - 1820 (2007/10/03)
Chiral C2-symmetric N-benzylazetidines have been conveniently prepared from optically pure anti-1,3-diols without loss of enantiomeric purity. N- Debenzylation led to the corresponding N-unsubstituted azetidines, which were then subjected to palladium-catalysed coupling reactions with aryl bromides to afford chiral N-arylazetidines. (R,R)-N-Benzyl-2,4-dimethylazetidine has been employed in the synthesis of a new cyclopalladated complex, which can be used, for instance, as a chiral recognition agent for phosphorus ligands.
Enantioselective synthesis ofanti 1, 3-diols via ru(ii)-catalyzed hydrogénations
Blanc, Delphine,Ratovelomanana-Vidai, Virginie,Marinetti, Angela,Genêt, Jean-Pierre
, p. 480 - 482 (2007/10/03)
The homogeneous ruthenium-catalyzed hydrogénation of new symmetrical 1, 3-diketones has been achieved with various ligands including SKEWPHOS and Me-DuPHOS. Complete conversions with enantiomeric and diastereomeric excesses up to 99% were obtained. This represents a new catalytic application of the chiral ligands above. Thieme Stuttgart.