Synthesis of N-Methyl L-Phenylalanine for Total Synthesis of Pepticinnamin E

摘要

The target compounds 3,10 and 11 were synthesized through different N-methylation strategies. The concise and efficient preparation of them in large scale was developed and 3,10 and 11 were obtained in suitable form used for both nitrogen-end and oxygen-end extension in next coupling reaction in peptides synthesis, specifically in total synthesis of natural pepticinnamin E.