Journal ArticleOPEN ACCESS

The use of carbon monoxide and imines as peptide derivative synthons: A facile palladium-catalyzed synthesis of α-amino acid derived imidazolines

Angewandte Chemie - International Edition (2001) 40(17) 3228-3230
DOI: 10.1002/1521-3773(20010903)40:17<3228::AID-ANIE3228>3.0.CO;2-Q
96Citations
Citations of this article
22Readers
Mendeley users who have this article in their library.
Get full text

Abstract

One of the most facile routes to prepare carboxylate-substituted imidazolines is by the palladium-catalyzed coupling of an imine, carbon monoxide, and an acid chloride. In this reaction, a peptide unit is constructed and directly incorporated into the heterocyclic core (se scheme).

Author supplied keywords

Cite

CITATION STYLE

APA

Dghaym, R. D., Dhawan, R., & Arndtsen, B. A. (2001). The use of carbon monoxide and imines as peptide derivative synthons: A facile palladium-catalyzed synthesis of α-amino acid derived imidazolines. Angewandte Chemie - International Edition, 40(17), 3228–3230. https://doi.org/10.1002/1521-3773(20010903)40:17<3228::AID-ANIE3228>3.0.CO;2-Q

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