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Literature DB >> 15602603

Application of tandem Ugi multi-component reaction/ring closing metathesis to the synthesis of a conformationally restricted cyclic pentapeptide.

Silvia Anthoine Dietrich¹, Luca Banfi, Andrea Basso, Gianluca Damonte, Giuseppe Guanti, Renata Riva.

Abstract

A conformationally restricted cyclic pentapeptide, containing an unsaturated 9-membered lactam as a semi-rigid scaffold, was prepared in a very convergent manner, through tandem Ugi reaction/ring closing metathesis.

Entities: Chemical

Mesh：

Substances：
Peptides, Cyclic

Year: 2004 PMID： 15602603 DOI： 10.1039/b414374d

Source DB: PubMed Journal: Org Biomol Chem ISSN： 1477-0520 Impact factor: 3.876

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Cited

2 in total

Review 1. Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics.

Authors: Gijs Koopmanschap; Eelco Ruijter; Romano Va Orru
Journal: Beilstein J Org Chem Date: 2014-03-04 Impact factor: 2.883

2. Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics.

Authors: Thimmalapura M Vishwanatha; Enrico Bergamaschi; Alexander Dömling
Journal: Org Lett Date: 2017-06-05 Impact factor: 6.005

2 in total