64240-80-8Relevant articles and documents
4-Aminophenyldiphenylphosphinite (APDPP), a new heterogeneous and acid scavenger phosphinite - Conversion of alcohols, trimethylsilyl, and tetrahydropyranyl ethers to alkyl halides with halogens or N-halosuccinimides
Iranpoor, Nasser,Firouzabadi, Habib,Gholinejad, Mohammad
, p. 1006 - 1012 (2007/10/03)
A new heterogeneous phosphinite, 4-aminophenyldiphenylphosphinite (APDPP), is prepared and used for the efficient conversion of alcohols, trimethylsilyl ethers, and tetrahydropyranyl ethers to their corresponding bromides, iodides, and chlorides in the presence of molecular halogens or N-halosuccinimides. The amino group in this phosphinite acts as an acid scavenger and removes the produced acid. A simple filtration easily removes the phosphinate by-product.
CLEAVAGE OF CARBON-OXYGEN BONDS. DIMETHYLBORON BROMIDE. A NEW REAGENT FOR ETHER CLEAVAGE
Guindon, Yvan,Yoakim, Christiane,Morton, Howard E.
, p. 2969 - 2972 (2007/10/02)
A general and efficient procedure for the cleavage of aliphatic, aromatic and cyclic ethers by the use of dimethylboron bromide is described.