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DOI: 10.1055/s-0030-1260572
Development of Bicyclo[3.3.0]octadiene- or Dicyclopentadiene-Based Chiral Diene Ligands for Transition-Metal-Catalyzed Reactions
Publication History
Publication Date:
23 May 2011 (online)
Abstract
This account summarizes our efforts on the design, synthesis, and application of two classes of chiral diene ligands bearing bicyclo[3.3.0]octadiene or dicyclopentadiene skeletons. These chiral diene ligands can be readily prepared from inexpensive commercial materials with enzymatic resolution as the key synthetic step. The ligands have been successfully applied in some rhodium-catalyzed reactions, including 1,4-addition to α,β-unsaturated carbonyl compounds, arylation of imines, and conjugate addition to nitroalkenes. In addition, they have been used in the first successful palladium-diene-catalyzed asymmetric reaction.
1 Introduction
2 Preparation of Optically Active Chiral Diene Ligands
3 Preparation and X-ray Crystallography of Rhodium- and Palladium-Diene Complexes
4 Rhodium-Catalyzed Asymmetric Addition Reactions
4.1 Rhodium-Catalyzed Asymmetric Addition to α,β-Unsaturated Ketones and Esters
4.2 Rhodium-Catalyzed Asymmetric Addition to Imines
4.3 Rhodium-Catalyzed Asymmetric Addition to Nitroalkenes
4.4 Rhodium-Catalyzed Asymmetric Addition to α,β-Unsaturated γ-Lactams
5 Palladium-Catalyzed Asymmetric Suzuki-Miyaura Cross-Coupling Reactions
6 Summary and Outlook
Key words
asymmetric catalysis - diene complexes - Michael additions - cross-coupling - rhodium
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