92148-47-5Relevant articles and documents
Highly Chemoselective gem-Difluoropropargylation of Aliphatic Alcohols
Okamura, Toshitaka,Egoshi, Syusuke,Dodo, Kosuke,Sodeoka, Mikiko,Iwabuchi, Yoshiharu,Kanoh, Naoki
supporting information, p. 16002 - 16006 (2019/11/19)
Despite the potential of α-fluoroethers in medicinal chemistry, their synthetic methods, especially etherification of aliphatic alcohols, have been limited. Herein, we developed two- and three-step gem-difluoropropargylation of aliphatic alcohols includin
An efficient and selective deprotection of tetrahydropyranyl ethers by CeCl3.7H2O
Reddy,Neelakantan,Iyengar
, p. 4107 - 4111 (2007/10/03)
Treatment of tetrahydropyranyl ethers with cerium (III) chloride heptahydrate in methanol provides a simple, convenient and selective method for detetrahydropyranylation, and the parent alcohols are obtained in high yields.