1127547-40-3Relevant articles and documents
BF3-OEt2-mediated rearrangement of (4-phenylpiperidin-4-yl)-arylmethanols
Chang, Meng-Yang,Wu, Tsun-Cheng,Lin, Shiang-Tsern
, p. 468 - 473 (2008/12/23)
Synthesis of several 4-benzhydrylidenepiperidine analogs has been established starting from different (4-phenylpiperidin-4-yl)-arylmethanols via boron trifluoride etherate mediated rearrangement. The possible rearranged mechanism was proposed. Boron trifluoride etherate-mediated rearrangement of the related derivatives was also examined. It presents a novel rearrangement reaction catalyzed by boron trifluoride etherate and broadens the scope of application.