604767-06-8Relevant academic research and scientific papers
A conceptually new approach to the asymmetric synthesis of 3-aryl and alkyl poly-substituted isoindolinones
Deniau, Eric,Couture, Axel,Grandclaudon, Pierre
experimental part, p. 2735 - 2740 (2009/04/07)
A conceptually new and efficient asymmetric synthesis of C-3 arylated or alkylated poly-substituted isoindolinones is reported. The key step is the diastereoselective reduction of an N-acylhydrazonium species derived from the previously assembled corresponding hydroxyl derivative bearing the (S)-2-methoxymethylpyrrolidine (SMP) auxiliary.
A new synthetic route to highly enantioenriched 3-substituted-2,3-dihydro-1H-isoindol-1-ones
Deniau, Eric,Enders, Dieter,Couture, Axel,Grandclaudon, Pierre
, p. 2253 - 2258 (2007/10/03)
A concise and efficient synthesis of highly enantioenriched 3-alkyl and 3-aryl-2,3-dihydro-1H-isoindolinones is reported. The key step relies on the diastereoselective reduction of the N-acylhydrazonium salts generated by acidic treatment of hemiaminal precursors bearing the (S)-2-methoxymethylpyrrolidin-1-yl (SMP) auxiliary.
