A novel approach for the synthesis of unprecedented C3-mono-functionalized indolin-2-ones is reported, starting from 2-oxindole and chalcones. The reactions proceed regioselectively under mild conditions, without di- and tri-alkylated side products. The new compounds have been evaluated in vitro for their antiproliferative effects against the protozoan Leishmania infantum. Interestingly, they appear able to kill L. infantum promastigotes and amastigotes, without significant cytotoxic effects.
|Data di pubblicazione:||2014|
|Titolo:||Direct synthesis of C3-mono-functionalized oxindoles from N-unprotected 2-oxindole and their antileishmanial activity|
|Citazione:||Scala, A., Cordaro, M., Grassi, G., Piperno, A., Barberi, G., Cascio, A., et al. (2014). Direct synthesis of C3-mono-functionalized oxindoles from N-unprotected 2-oxindole and their antileishmanial activity. BIOORGANIC & MEDICINAL CHEMISTRY, 22, 1063-1069.|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.1016/j.bmc.2013.12.039|
|Appare nelle tipologie:||1.01 Articolo in rivista|