Solution phase synthesis of a spiro[pyrrolidine-2,3′-oxindole] library via a three component 1,3-dipolar cycloaddition reaction
- 1 April 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (16) , 2235-2238
- https://doi.org/10.1016/s0040-4039(98)00234-2
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Synthetic Design for Combinatorial Chemistry. Solution and Polymer-Supported Synthesis of Polycyclic Lactams by Intramolecular Cyclization of Azomethine YlidesJournal of the American Chemical Society, 1997
- Combinatorial Synthesis of Small Organic MoleculesAngewandte Chemie International Edition in English, 1996
- A short dipolar cycloaddition approach to γ-lactam alkaloids from cynometra hankeiTetrahedron Letters, 1996
- Multiple-Component Condensation Strategies for Combinatorial Library SynthesisAccounts of Chemical Research, 1996
- Synthesis and Applications of Small Molecule LibrariesChemical Reviews, 1996
- XY–ZH systems as potential 1,3-dipoles. Part 12. Mechanism of formation of azomethine ylides via the decarboxylative route from α-amino acidsJournal of the Chemical Society, Perkin Transactions 1, 1988
- Iminium ion route to azomethine yields from primary and secondary aminesJournal of the Chemical Society, Chemical Communications, 1986
- Decarboxylative transamination. A new route to spirocyclic and bridgehead-nitrogen compounds. Relevance to α-amino acid decarboxylasesJournal of the Chemical Society, Chemical Communications, 1984
- Decarboxylative transamination. Mechanism and applications to the synthesis of heterocyclic compoundsJournal of the Chemical Society, Chemical Communications, 1984