FeCl3-Mediated Reaction of Alkynols with Iodine: An Efficient and Convenient Synthetic Route to Vinyl Iodides
摘要:
[image omitted] The FeCl3-mediated reaction of alkynols with iodine resulted in intramolecular addition of hydroxyl to alkyne to produce a wide range of iodocycloenol ethers in good to excellent yields under mild reaction conditions. On the other hand, 1,2-diiodides were obtained in good yields when propargyl alcohol reacted with iodine in the same condition.
FeCl<sub>3</sub>-Mediated Reaction of Alkynols with Iodine: An Efficient and Convenient Synthetic Route to Vinyl Iodides
作者:Lei Su、Chun-Yan Lei、Wei-Yong Fan、Liang-Xian Liu
DOI:10.1080/00397911.2010.481739
日期:2011.3.28
[image omitted] The FeCl3-mediated reaction of alkynols with iodine resulted in intramolecular addition of hydroxyl to alkyne to produce a wide range of iodocycloenol ethers in good to excellent yields under mild reaction conditions. On the other hand, 1,2-diiodides were obtained in good yields when propargyl alcohol reacted with iodine in the same condition.