Title of article :
Highly enantioselective synthesis of 3-cycloalkanone-3-hydroxy-2-oxindoles, potential anticonvulsants
Author/Authors :
Raj، نويسنده , , Monika and Veerasamy، نويسنده , , Nagarathanam and Singh، نويسنده , , Vinod K.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2010
Pages :
3
From page :
2157
To page :
2159
Abstract :
Highly enantioselective catalytic synthesis of 3-cycloalkanone-3-hydroxy-2-oxindoles was achieved by using primary-tertiary diamine-Brّnsted acid catalyst in both organic medium and aqueous medium. The products, thus obtained act as potential anticonvulsants.
Keywords :
aldol reaction , Aqueous medium , organocatalyst , enantioselective reaction , ANTICONVULSANTS
Journal title :
Tetrahedron Letters
Serial Year :
2010
Journal title :
Tetrahedron Letters
Record number :
1871976
Link To Document :
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