153446-74-3Relevant academic research and scientific papers
One-pot synthesis of 3-haloflavones from flavones using Oxone and potassium halide as a halogenation reagent
Peng, Tao,Wang, Gang,Zhang, Shouguo,Sun, Yunbo,Liu, Shuchen,Wang, Lin
, (2019/12/27)
A two-step, one-pot method has been developed for the synthesis of 3-haloflavones from the corresponding flavones. The method uses Oxone and potassium halide to produce the active molecular halogen in situ. The solvent (methanol) then participates in the reaction to afford the 2-methoxy-3-haloflavanone derivative. After adding sodium hydroxide, the corresponding 3-haloflavone product is obtained in good to excellent yields. This method provides a convenient synthesis of 3-chloro, 3-bromo and 3-iodo flavones from the same flavone starting material.
Diversity-oriented synthesis of 3-iodochromones and heteroatom analogues via ICl-induced cyclization
Zhou, Chengxiang,Dubrovsky, Anton V.,Larock, Richard C.
, p. 1626 - 1632 (2007/10/03)
The ICl-induced cyclization of heteroatom-substituted alkynones provides a simple, highly efficient approach to various 3-iodochromones and analogues. This process is run under mild conditions, tolerates various functional groups, and generally provides chromones in good to excellent yields. Subsequent palladium-catalyzed transformations afford a rapid increase in molecular complexity and a convenient preparation of a wide range of functionally substituted chromones, furans, and polycyclic compounds. Iodothiochromenones and iodoquinolinones are also prepared by similar ICl-induced cyclizations.
Synthesis of 3-iodo derivatives of flavones, thioflavones and thiochromones
Zhang,Li
, p. 565 - 567 (2007/10/02)
The title compounds, 2-aryl-3-iodo-4H-1-benzopyrans and 2-alkyl or 2-aryl-3-iodo-4H-1-benzothiopyrans, were prepared by reaction of the corresponding heterocyclic derivatives with the iodine-cerium(IV) ammonium nitrate system under mild conditions. The scope and proposed mechanism of the reaction were also demonstrated.
