7706-86-7Relevant articles and documents
Rapid access to 4-substituted-pyrones and 2(5H)-furanones via a palladium-catalyzed C-OH bond activation
Hu, Yi,Ding, Qiuping,Ye, Shengqing,Peng, Yiyuan,Wu, Jie
supporting information; experimental part, p. 7258 - 7262 (2011/10/08)
An efficient palladium-catalyzed cross-coupling reaction of 4-hydroxy-pyrone or 4-hydroxy-2(5H)-furanone with arylboronic acid is described, which affords the 4-substituted-pyrones and 2(5H)-furanones in good yields. This transformation proceeds through a C-OH bond activation under mild conditions.
Palladium-catalyzed cross-coupling reactions of 4-tosyl-2(5H)-furanone with boronic acids: A facile and efficient route to generate 4-substituted 2(5H)-furanones
Wu, Jie,Zhu, Qiang,Wang, Lisha,Fathi, Reza,Yang, Zhen
, p. 670 - 673 (2007/10/03)
An efficient and facile synthesis of 4-substituted 2(5H)-furanones using palladium catalyzed cross-coupling reactions between 4-tosyl-2(5H)-furanone and boronic acids is reported herein.
An expedient palladium-mediated route to 3-arylfurans
Taniguchi, Takahiko,Nagata, Hiroshi,Kanada, Regina Mikie,Kadota, Kohei,Takeuchi, Miwako,Ogasawara, Kunio
, p. 67 - 71 (2007/10/03)
A facile route to 3-arylfurans has been developed by employing the Heck reaction between 2,5-dihydro-2,5-dimethoxyfuran and aryl iodides as the key step.
