Complementary synthetic approaches to constitutionally diverse N-aminoalkylated isoindolinones: Application to the synthesis of falipamil and 5-HT1A receptor ligand analogues
Different synthetic approaches for the elaboration of poly and diversely substituted isoindolinones tailed with constitutionally diverse aminoalkylated chains have been developed. The key step is based upon the preliminary assembly of the isoindolinone te
Lorion, Magali,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre
experimental part
p. 1897 - 1903
(2010/02/16)
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