Title of article :
2-(N-Methylanilino)-3-formylchromone—a versatile synthon for incorporation of chromone moiety in a variety of heterocyclic systems and macrocycles through reactions with bifunctional nucleophiles
Author/Authors :
Gurmit Singh Pahal، نويسنده , , Lakhwinder Singh، نويسنده , , M.P.S. Ishar، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
8
From page :
7883
To page :
7890
Abstract :
Reactions of 2-(N-methylanilino)-3-formylchromones with a number of bifunctional nucleophiles, involving substitution of N-methylanilino moiety and/or condensations with 3-formyl function have provided an easy access to a variety of potentially biologically active hetero-annelated chromones, novel macrocycles, and tetradentate ligands having intact chromone moiety.
Keywords :
Macrocycles , chromones , Condensation , addition–elimination , chromano-azepines , chromano-oxazepines , chromano-thiazapine , chromanopyrole , chromano-quinolines , chromanopyrazoles
Journal title :
Tetrahedron
Serial Year :
2002
Journal title :
Tetrahedron
Record number :
1083495
Link To Document :
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