56437-43-5Relevant articles and documents
Isolation of catalytic intermediates in hydroamination reactions: Insertion of internal alkynes into a zirconium-amido bond
Leitch, David C.,Turner, Courtney S.,Schafer, Laurel L.
supporting information; experimental part, p. 6382 - 6386 (2010/12/19)
Insert alkyne to continue: Reaction of a bis(ureate) zirconium dimethylamido complex with electron-rich alkynes leads to vinylamine insertion products (see scheme). The insertion of C=C unsaturated bonds into M=N bonds is proposed as a key step in lanthan
The reaction of arylaldehydes with hexamethylphosphorous triamide and the use of the resulting products for the synthesis of enamines and deoxybenzoins
Babudri,Fiandanese,Musio,Naso,Sciavovelli,Scilimati
, p. 225 - 228 (2007/10/02)
The reaction between the arylaldehydes 1a,b and hexamethylphosphorous triamide 2 leads to the [aryl(dimethylamino)methyl]phosphonic bis(dimethylamides) 3a,b. These can be easily deprotonated by butyllithium in 1,2-dimethoxyethane and condensed with arylaldehydes to afford enamines 4a-f or deoxybenzoins 5a-f in fair to good yield.