A Catalytic Multicomponent Approach for the Stereoselective Synthesis of cis‐4,5‐Disubstituted Pyrrolidinones and Tetrahydro‐3H‐pyrrolo[3,2‐c]quinolines
- 27 March 2012
- journal article
- research article
- Published by Wiley in Angewandte Chemie
- Vol. 51 (19), 4722-4725
- https://doi.org/10.1002/anie.201107831
Abstract
No abstract availableThis publication has 60 references indexed in Scilit:
- Synthesis of Diverse Lactam Carboxamides Leading to the Discovery of a New Transcription‐Factor InhibitorAngewandte Chemie, 2007
- Synthesis of Diverse Lactam Carboxamides Leading to the Discovery of a New Transcription‐Factor InhibitorAngewandte Chemie, 2007
- 4,5-Disubstituted cis-pyrrolidinones as inhibitors of type II 17β-hydroxysteroid dehydrogenase. Part 3. Identification of lead candidateBioorganic & Medicinal Chemistry Letters, 2006
- Hox genes: a continuation of embryonic patterning?Trends in Genetics, 2006
- Stereoselective γ-lactam synthesis via palladium-catalysed intramolecular allylationChemical Communications, 2005
- Surprisingly Mild “Enolate-Counterion-Free” Pd(0)-Catalyzed Intramolecular Allylic AlkylationsOrganic Letters, 2005
- The pathophysiology of HOX genes and their role in cancerThe Journal of Pathology, 2005
- The effects of (-)clausenamide on functional recovery in transient focal cerebral ischemiaNeurological Research, 2002
- Novel inhibitors of HIV protease: design, synthesis and biological evaluation of picomolar inhibitors containing cyclic P1/P2 scaffoldsBioorganic & Medicinal Chemistry Letters, 2000
- 3,3-Dialkyl- and 3-Alkyl-3-Benzyl-Substituted 2-Pyrrolidinones: A New Class of Anticonvulsant AgentsJournal of Medicinal Chemistry, 1996