Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenols, and aldehydes. The acetylation of 1° and 2° alcohols, diols, and phenols proceeded smoothly with 2.0 mol % of catalyst. However, the reaction worked well with only a few 3° alcohols. The methodology was also applicable to the synthesis of a few benzoate esters but required the use of 5.0 mol % catalyst. Aldehydes could also be converted into the corresponding 1,1-diesters (acylals) under the reaction conditions. Iron(III) tosylate is an inexpensive, and easy to handle, commercially available catalyst
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenol...
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenol...
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenol...
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenol...
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenol...
Lanthanide(III) complexes of p-toluenesulfonic acid (Ln(TOS)3) were prepared, characterized, and exa...
Iron(III) p-toluenesulfonate, Fe(OTs)3.6H20, is an inexpensive, versatile and commercially available...
Iron(III) p-toluenesulfonate, Fe(OTs)3.6H20, is an inexpensive, versatile and commercially available...
Iron(III) p-toluenesulfonate, Fe(OTs)3.6H20, is an inexpensive, versatile and commercially available...
Iron(III) p-toluenesulfonate, Fe(OTs)3.6H20, is an inexpensive, versatile and commercially available...
Iron(III) p-toluenesulfonate, Fe(OTs)3.6H20, is an inexpensive, versatile and commercially available...
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenol...
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenol...
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenol...
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenol...
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenol...
Lanthanide(III) complexes of p-toluenesulfonic acid (Ln(TOS)3) were prepared, characterized, and exa...
Iron(III) p-toluenesulfonate, Fe(OTs)3.6H20, is an inexpensive, versatile and commercially available...
Iron(III) p-toluenesulfonate, Fe(OTs)3.6H20, is an inexpensive, versatile and commercially available...
Iron(III) p-toluenesulfonate, Fe(OTs)3.6H20, is an inexpensive, versatile and commercially available...
Iron(III) p-toluenesulfonate, Fe(OTs)3.6H20, is an inexpensive, versatile and commercially available...
Iron(III) p-toluenesulfonate, Fe(OTs)3.6H20, is an inexpensive, versatile and commercially available...
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...
The deprotection of aromatic as well as conjugated acetals and ketals in water is catalyzed by iron(...