51751-33-8Relevant articles and documents
An Improved Synthesis of 2-Methylchromone-3-carboxylic Acid and its Esters
Coppola, Gary M.,Dodsworth, Roy W.
, p. 523 - 524 (1981)
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On-Water Cp?Ir(III)-catalyzed C-H functionalization for the synthesis of chromones through annulation of salicylaldehydes with diazo-ketones
Debbarma, Suvankar,Sk, Md Raja,Modak, Biswabrata,Maji, Modhu Sudan
, (2019/05/22)
A high-valent Ir(III)-catalyzed C-H bond functionalization is carried out for the first time on water for the synthesis of a biologically relevant chromone moiety. The C-H activation and annulation of salicylaldehydes with diazo-compounds provided the desired chromones. The synthesis of C3-substitution-free chromones has also been demonstrated by a one-pot decarboxylation by employing tert-butyl diazoester. C3 and C5 C-H activations of the product chromone are also carried out under different conditions for further diversification.
Cp?Ir(III)-Catalyzed C-H/O-H Functionalization of Salicylaldehydes for the Synthesis of Chromones at Room Temperature
Lade, Dhanaji M.,Aher, Yogesh N.,Pawar, Amit B.
, p. 9188 - 9195 (2019/08/12)
Herein, we report Cp Ir(III)-catalyzed C-H/O-H-bond functionalization of salicylaldehydes with α-diazocarbonyl compounds for the synthesis of chromones under redox-neutral conditions. The reaction proceeds at room temperature and displays excellent functi