139373-54-9Relevant articles and documents
Non-dehydrative pinacol rearrangement using a Lewis acid-trialkyl orthoester combined system
Kita, Yasuyuki,Yoshida, Yutaka,Mihara, Sachiko,Furukawa, Akihiro,Higuchi, Kazuhiro,Fang, Dai-Fei,Fujioka, Hiromichi
, p. 14689 - 14704 (2007/10/03)
An efficient pinacol rearrangement mediated by trialkyl orthoformate has been developed. The reactions of various types of diols with a catalytic amount of a Lewis acid in the presence of an orthoester afforded the rearranged product in good yields via a cyclic orthoester intermediate. This combined system is applicable not only to cyclic and acyclic tri- and tetra- substituted diols but also to the diols having acid-sensitive acetals.
The Catalytic Pinacol Rearrangement of 1,2-Diols Using an Antimony(V)Salt
Harada, Tsunehiro,Mukaiyama, Teruaki
, p. 81 - 84 (2007/10/02)
In the presence of a catalytic amount of antimony(V)chloride or antimony(V)salt generated from antimony(V)chloride and silver hexafluoroantimonate, the pinacol rearrangement of several 1,2-diols or their trimethylsilyl ethers proceeds smoothly to give the corresponding ketones in good yields.