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DOI: 10.1055/s-2007-977434
Cation-Exchanged Montmorillonites as Solid Acid Catalysts for Organic Synthesis
Publication History
Publication Date:
13 April 2007 (online)
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Abstract
In this account the authors review a novel approach to design high-performance heterogeneous acid catalysts using montmorillonites as macroligands of active metal species for various C-C bond formations and one-pot syntheses. The catalytic systems using the above heterogeneous catalysts offer significant benefits in achieving environmentally friendly organic syntheses aiming towards green and sustainable chemistry. Furthermore, the present preparation method for the immobilization of metal species within the interlayer space is strikingly simple and allows a strong protocol for creating various nanostructured and functionalized metal-cation catalysts.
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1 Introduction
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2 Preparation and Characterization of Montmorillonite-Enwrapped Cation Species
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2.1 Ti4+-mont and H+-mont as Brønsted Acids
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2.2 Cu2+-mont and Sc3+-mont as Lewis Acids
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3 Brønsted Acid Catalyzed Reactions
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3.1 Aromatic Alkylation Using Ti4+-mont Catalyst
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3.2 Miscellaneous Functional Group Transformations Using Ti4+-mont Catalyst
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3.3 Addition of 1,3-Dicarbonyls to Olefins Catalyzed by
H+-mont Catalyst -
4 Lewis Acid Catalyzed C-C Bond-Forming Reactions
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4.1 Michael Reaction Using Cu2+-mont Catalyst
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4.2 Sakurai-Hosomi and Diels-Alder Reactions Catalyzed by Cu2+-mont
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4.3 Michael Reactions in Water Using Sc3+-mont Catalyst
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5 One-Pot Synthesis Using Solid Acid and Base Catalysts
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6 Conclusions
Key words
montmorillonites - solid acids - C-C bond-forming reactions - one-pot synthesis
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