Solvent-free synthesis of peptides

193Citations
Citations of this article
122Readers
Mendeley users who have this article in their library.

Abstract

Chamical Equation Presentation A crush on sweetness! The coupling of a urethane-protected N-carboxyanhydride of an amino acid with another amino acid derivative under ball-milling conditions gives a protected dipeptide in very high yield (see scheme; PG: protecting group). The reaction takes place in the solid state. The synthesis was applied to the preparation of a tri peptide and the sweetener aspartame, without any organic solvent or purification. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.

Cite

CITATION STYLE

APA

Declerck, V., Nun, P., Martinez, J., & Lamaty, F. (2009). Solvent-free synthesis of peptides. Angewandte Chemie - International Edition, 48(49), 9318–9321. https://doi.org/10.1002/anie.200903510

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free