Diversity oriented and chemoenzymatic synthesis of densely functionalized pyrrolidines through a highly diastereoselective Ugi multicomponent reaction

Highly Stereoselective Synthesis of Substituted Prolyl Peptides Using a Combination of Biocatalytic Desymmetrization and Multicomponent Reactions

(2010) Anass Znabet et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

A Highly Convergent Synthesis of Tricyclic N-Heterocycles Coupling an Ugi Reaction with a Tandem SN2′-Heck Double Cyclization

(2010) Renata Riva et al.   JOURNAL OF ORGANIC CHEMISTRY

Emerging molecular diversity from the intra-molecular Ugi reaction: iterative efficiency in medicinal chemistry

(2009) Christopher Hulme et al.   MOLECULAR DIVERSITY

Fragment-based ligand discovery

(2009) M. Fischer et al.   MOLECULAR INTERVENTIONS

Application of an Ugi type reaction to an N-silyl-4,4-disubstituted 1,4-dihydropyridine

(2009) Christian A. Sperger et al.   TETRAHEDRON

Three-component Ugi–Smiles couplings of cyclic imines

(2009) Laurent El Kaïm et al.   TETRAHEDRON LETTERS

Molecular diversity in the context of leadlikeness: compound properties that enable effective biochemical screening

(2008) Gilbert M Rishton   CURRENT OPINION IN CHEMICAL BIOLOGY

The Effect of Lewis Acids on the Stereochemistry in the Ugi Three-Component Reaction withD-lyxo-Pyrroline

(2008) Kimberly M. Bonger et al.   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Polyfunctionalized Pyrrolidines by Ugi Multicomponent Reaction Followed by Palladium-Mediated SN2‘ Cyclizations

(2008) Luca Banfi et al.   JOURNAL OF ORGANIC CHEMISTRY

A convergent synthesis of enantiopure bicyclic scaffolds through multicomponent Ugi reaction

(2007) Luca Banfi et al.   TETRAHEDRON