Efficient paper and Practical Procedure for the Esterification of the Free α-Car- boxylic Acid of Amino Acid Residues with β-(Trimethylsilyl)ethoxymethyl Chloride and Triisopropylsilyl Chloride
Résumé
An efficient and practical procedure for the free α-carboxylic acid esterification of amino acid residues with β-(trimethyl- silyl)ethoxymethyl chloride and triisopropylsilyl chloride is described. The reaction takes place under mild conditions and the expected protected amino acids are obtained in good to excellent yields. Our method provides a useful alternative for the C-terminal carboxylic acid protection of amino acids and peptides. Moreover, the removal of such protection was also achieved under mild condi- tions, without affecting either the other protecting groups at the α- amino moiety and side chains or the optical integrity at the α-posi- tion of the amino acid residues. Examples of their use in peptide synthesis are also illustrated.