76369-11-4Relevant academic research and scientific papers
A versatile route to 2-alkyl-/aryl-amino-3-formyl- and hetero-annelated-chromones, through a facile nucleophilic substitution at C2 in 2-(N-methylanilino)-3-formylchromones
Singh, Gurmit,Singh, Rajinder,Girdhar, Navdeep K,Ishar
, p. 2471 - 2480 (2007/10/03)
The N-methylanilino group in 2-(N-methylanilino)-3-formylchromones, obtained in high yield by rearrangement of C(4-oxo-4H[1]-benzopyran-3-yl)-N-phenylnitrones to 2-anilino-3-formyl-chromones followed by N-methylation, undergoes facile nucleophilic substitution by a variety of nitrogen nucleophiles, thereby paving the way for synthesis of a variety of novel 2-substituted-3-formylchromone derivatives as well as hetero-annelated chromones.
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
Singh, Gurmit,Singh, Lakhwinder,Ishar
, p. 7883 - 7890 (2007/10/03)
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.
Hetericyclic Systems. Part 14. Condensation Reactions of 2-(4-Oxo-4H-1-benzopyran-3-yl)-1,3-dioxolane
Ghosh, Chandra Kanta,Bandyopadhyay, Chandrakanta,Morin, Christophe
, p. 1989 - 1994 (2007/10/02)
Nitrogen nucleophiles under 1,4-addition with the title acetal (4; R=H, Me, and Cl) to give an intermediate that ultimately produces in most cases the same product as is obtained from the corresponding aldehyde (3) under similar conditions.Thus, compound
