Magnesium iodide promoted defluorinative reactions of 2,2-difluorocyclopropyl aryl ketones with aryl imines: A new, general synthesis of 2-alkylideneazetidines
摘要:
Upon treatment with anhydrous MgI2, 2,2-difluorocyclopropyl aryl ketones undergo a ring-opening process leading to complete loss of fluorine. When carried out in the presence of aryl imines, the reaction leads to a novel synthesis of 2-alkylideneazetidenes. A fluorine-free allenyl ketone is proposed as an intermediate in these reactions. (C) 2010 Published by Elsevier B.V.
Magnesium iodide promoted defluorinative reactions of 2,2-difluorocyclopropyl aryl ketones with aryl imines: A new, general synthesis of 2-alkylideneazetidines
作者:Wei Xu、Ion Ghiviriga、Qing-Yun Chen、William R. Dolbier
DOI:10.1016/j.jfluchem.2010.06.021
日期:2010.9
Upon treatment with anhydrous MgI2, 2,2-difluorocyclopropyl aryl ketones undergo a ring-opening process leading to complete loss of fluorine. When carried out in the presence of aryl imines, the reaction leads to a novel synthesis of 2-alkylideneazetidenes. A fluorine-free allenyl ketone is proposed as an intermediate in these reactions. (C) 2010 Published by Elsevier B.V.