Enantioselective rauhut-currier-type cyclizations via dienamine activation: scope and mechanism

This Feature Article describes our mechanistic studies in organocatalytic Rauhut-Currier-type reactions and some applications in target-oriented synthesis. The developed approach involves the cyclization of two tethered Michael acceptors via dienamine intermediates and leads to highly functionalized...

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Bibliographic Details
Authors: Marqués-López, Eugenia, Herrera, Raquel P., Marks, Timo, Jacobs, Wiebke C., Christmann, Mathias
Format: article
Status:Versión aceptada para publicación
Publication Date:2013
Country:España
Institution:Consejo Superior de Investigaciones Científicas (CSIC)
Repository:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/111174
Online Access:http://hdl.handle.net/10261/111174
Access Level:Open access
Keyword:Asymmetric synthesis
Michael addition
Dienamine activation
Rauhut–Currier reaction
Organocatalysis
Description
Summary:This Feature Article describes our mechanistic studies in organocatalytic Rauhut-Currier-type reactions and some applications in target-oriented synthesis. The developed approach involves the cyclization of two tethered Michael acceptors via dienamine intermediates and leads to highly functionalized cycloalkenes. The utility of these intermediates is further demonstrated by the synthesis of biologically important targets, such as optically active iridoid derivatives. 1 Introduction 2 Organocatalytic Cyclization of Tethered α,β-Unsaturated Carbonyl Compounds; Synthesis of Cyclopentene Derivatives 2.1 Mechanistic Proposal 2.1.1 ESI-HRMS Measurements 2.1.2 NMR Experiments 2.1.3 Complementary Reactivity 2.2 Synthetic Applications 3 Organocatalytic Cyclization of Tethered α,β-Unsaturated Carbonyl Compounds; Synthesis of Cyclohexene Derivatives 4 Conclusions. © Georg Thieme Verlag Stuttgart New York.