Abstract
Boc- or Z-amino acids were conveniently amidated at room temperature by a one-pot procedure employing ammonium hydrogencarbonate and N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline in yields of 81–96%. The benzyl ester-type protector for the side chains of aspartic acid and glutamic acid was not affected by the procedure.
Cite
CITATION STYLE
APA
Nozaki, S., & Muramatsu, I. (1988). Convenient Synthesis of N -Protected Amino Acid Amides. Bulletin of the Chemical Society of Japan, 61(7), 2647–2648. https://doi.org/10.1246/bcsj.61.2647
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free