Abstract
Amide formation from amino acids was achieved in an easy and convenient one‐pot procedure using di‐tert‐butyl dicarbonate both as a protecting and an activating agent. A number of dipeptides have been synthesized in good yields.
Acknowledgments
We thank J. Joule (Manchester University) for obtaining the mass spectra. We thank both J. Joule and B. Novak and for their constructive comments.