Addition of TMSCN to chiral ketimines derived from isatin. Synthesis of an oxindole-based peptidomimetic and a bioactive spirohydantoin

Enantioselective Organocatalytic Strecker Reactions in the Synthesis of α-Amino Acids

(2010) Jürgen Martens   ChemCatChem

A facile method for the synthesis of oxindole based quaternary α-aminonitriles via the Strecker reaction

(2010) Yun-Lin Liu et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

The spiropiperidine-3,3′-oxindole scaffold: a type II β-turn peptide isostere

(2010) Giordano Lesma et al.   TETRAHEDRON

Tetrahydroisoquinoline-Based Spirocyclic Lactam as a Type II′ β-Turn Inducing Peptide Mimetic

(2009) Giordano Lesma et al.   JOURNAL OF ORGANIC CHEMISTRY

Grignard Addition to Imines Derived from Isatine: A Method for the Asymmetric Synthesis of Quaternary 3-Aminooxindoles

(2009) Giordano Lesma et al.   JOURNAL OF ORGANIC CHEMISTRY

Ruthenium N-heterocyclic carbene catalysts for selective reduction of nitriles to primary amines

(2009) Daniele Addis et al.   TETRAHEDRON LETTERS

The Catalytic Asymmetric Strecker Reaction: Ketimines Continue to Join the Fold

(2008) Stephen J. Connon   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Solution-phase synthesis of 2-cyano and 2-amido aziridinyl peptides

(2008) Stefania Fioravanti et al.   TETRAHEDRON