244104-71-0Relevant articles and documents
Diastereoselective synthesis of 4-substituted 5-(p-tolylsulfinyl)-5,6-dehydropiperidin-2-ones. A new approach to methyl L-(2S,4S)-4-methyl-6-oxopipecolate
Acherki, Hassan,Alvarez-Ibarra, Carlos,De Dios, Alfonso,Gutierrez, Marta,Quiroga, Maria L.
, p. 3173 - 3183 (2007/10/03)
The sulfoxide-mediated diastereoselective Michael reaction of homochiral α-sulfinylketimines 1a-d and β-substituted ene esters 2a-d (Hua's reaction) was explored. Straightforward cyclization of the open-chain adducts take place under the reaction conditions to provide the 4-substituted 5-(p-tolylsulfinyl)-5,6-dehydropiperidin-2-ones 3 and 7-12, whose stereochemistry is formed in the prior step. Furthermore, the role of the metal ion of the aza-enolate reagents and the steric demands of the O-alkyl ester group have been examined. It seems that the anti-diastereoselectivity depends on metal chelation by the oxygen of the ester as well as the oxygen of the sulfinyl group and the nitrogen in the aza-enolate ((Z)-configuration). In addition, the synthesis of methyl L-(2S,4S)-4-methyl-6-oxopipecolate has been achieved from the suitably functionalized 2-sulfinylketimine 1a (five steps; overall yield: 53-65%).
Sulfoxide-mediated diastereoselective Michael additions. New enantioselective synthesis of C-4 substituted 2-pyroaminoadipic acids
Acherki, Hassan,Alvarez-Ibarra, Carlos,Barrasa, Alicia,De Dios, Alfonso
, p. 5763 - 5766 (2007/10/03)
Diastereoselective reactions of suitably functionalized homochiral β-iminosulfoxides with Michael acceptors provide a new and efficient route for the asymmetric synthesis of C-4 substituted 2-pyroaminoadipates. Extension of the scope of the sulfoxide-mediated aza-enolate conjugate addition (Hua's reaction) has also been explored.
