873211-41-7Relevant articles and documents
Magnesium dicarboxylates promote the prenylation of phenolics that is extended to the total synthesis of icaritin
Fu, Xuewen,Lu, Xiaoxia,Wang, Chun,Wen, Yongju,Xiong, Wei,Zhang, Guolin,Zhang, Jichao
, p. 1117 - 1124 (2022/02/16)
The prenylation of phenolic substrates promoted by magnesium dicarboxylates was developed. An investigation of the scope demonstrated that substrates with electron-donating group(s) gave better yields than those with electron-withdrawing group(s). Althoug
Synthesis of?compounds with antiproliferative activity as?analogues of?prenylated natural products existing in?Brazilian propolis
Pisco, Laura,Kordian, Marcus,Peseke, Klaus,Feist, Holger,Michalik, Dirk,Estrada, Ernesto,Carvalho, Jo?o,Hamilton, Gerhard,Rando, Daniela,Quincoces, Jose
, p. 401 - 407 (2007/10/03)
This work describes the syntheses and antitumoral properties of five prenyl compounds from which antiproliferative activities were predicted by using the TOPS-MODE approach, a computational method for drug design. The syntheses of 2-(3-methylbut-2-enyloxy
Bismuth triflate catalyzed [1,3] rearrangement of aryl 3-methylbut-2-enyl ethers
Ollevier, Thierry,Mwene-Mbeja, Topwe M.
, p. 3963 - 3966 (2008/03/11)
An efficient bismuth triflate catalyzed [1,3] rearrangement of aryl 3-methylbut-2-enyl ethers has been developed. The reaction proceeds rapidly and affords the corresponding para- and ortho-prenylated phenols and naphthols in moderate to good yields (up t
