Synthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indoles
An acid-assisted [4 + 1]-cycloaddition of indoles with nitrostyrenes affords 4′H-spiro[indole-3,5′-isoxazoles] in a diastereomerically pure form. Several of these spirocyclic molecules exhibit promising anticancer activity by reducing viability and inducing differentiation of neuroblastoma cells
Sábháilte in:
Míreanna comhchosúla
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Preparation of spiro[indole-3,5′-isoxazoles] via Grignard conjugate addition/spirocyclization sequence
de réir: Aksenov, A. V., et al.
Foilsithe / Cruthaithe: (2021) -
Reductive Cleavage of 4′ H-Spiro[indole-3,5′-isoxazoles] en Route to 2-(1 H-Indol-3-yl)acetamides with Anticancer Activities
de réir: Aksenov, A. V., et al.
Foilsithe / Cruthaithe: (2022) -
Direct reductive coupling of indoles to nitrostyrenes en route to (indol-3-yl)acetamides
de réir: Aksenov, A. V., et al.
Foilsithe / Cruthaithe: (2018) -
Preparation of stereodefined 2-(3-Oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenes
de réir: Aksenov, A. V., et al.
Foilsithe / Cruthaithe: (2019) -
Unexpected cyclization of 2-(2-aminophenyl)indoles with nitroalkenes to furnish indolo[3,2-: C] quinolines
de réir: Aksenov, A. V., et al.
Foilsithe / Cruthaithe: (2018)