98210-62-9Relevant academic research and scientific papers
Convenient and efficient preparation of N-protected (α-aminoacyl)oxy- substituted terpenes and alkanes
Katritzky, Alan R.,Angrish, Parul
, p. 4135 - 4142 (2008/03/13)
Chiral N-protected (α-aminoacyl)oxy-substituted terpenes and alkanes, including diastereomeric analogues, are conveniently and efficiently prepared from the corresponding readily available chiral and racemic 1- {[(benzyloxycarbonyl)amino]acyl}benzotriazol
1,1'-Carbonylbis(3-methylimidazolium) Triflate: An Efficient Reagent for Aminoacylations
Saha, Ashis K.,Schultz, Peter,Rapoport, Henry
, p. 4856 - 4859 (2007/10/02)
Amino acid carboxyl activation and subsequent coupling with nucleophiles frequently suffer from uncertain risks of racemization, complex reagent preparation, or troublesome side-product removal.All of these difficulties are eliminated with a new, simple reagent, 1,1'-carbonylbis(3-methylimidazolium) triflate (CBMIT), obtainable readily by bis-alkylation of carbonyldiimidazole with methyl triflate.Via a highly reactive acyl imidazolium intermediate, CBMIT couples amino acid components or amino acids and alcohols to give peptides and esters, easily isolated in high yield.The reaction medium remains free of any base, and no loss of optical activity is observed.
