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Journal ArticleDOI

Asymmetric enamine catalysis.

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This article is published in Chemical Reviews.The article was published on 2007-12-12. It has received 2308 citations till now. The article focuses on the topics: Enamine & Hajos–Parrish–Eder–Sauer–Wiechert reaction.

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Citations
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Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis

TL;DR: The conversion of these bench stable, benign catalysts to redox-active species upon irradiation with simple household lightbulbs represents a remarkably chemoselective trigger to induce unique and valuable catalytic processes.
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The advent and development of organocatalysis

TL;DR: My opinion on why the field of organocatalysis has blossomed so dramatically over the past decade is presented.
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Solar Synthesis: Prospects in Visible Light Photocatalysis

TL;DR: A variety of reaction types have now been shown to be amenable to visible light photocatalysis via photoinduced electron transfer to or from the transition metal chromophore, as well as energy-transfer processes.
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Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C‐3 Position

TL;DR: The catalytic asymmetric synthesis of the tetrasubstituted carbon stereocenter at the C-3 position of the oxindole framework integrates new synthetic methods and chiral catalysts.
References
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Journal ArticleDOI

Proline-Catalyzed Direct Asymmetric Aldol Reactions

TL;DR: The finding that the amino acid proline is an effective asymmetric catalyst for the direct aldol reaction between unmodified acetone and a variety of aldehydes is reported.
Journal ArticleDOI

In the Golden Age of Organocatalysis

TL;DR: The diverse examples show that in recent years organocatalysis has developed within organic chemistry into its own subdiscipline, whose "Golden Age" has already dawned.
Journal ArticleDOI

Enamine-Based Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and Diels−Alder Reactions

TL;DR: The contributions of this laboratory to converting enzymatic enamines, and in some cases imines, into a versatile catalytic asymmetric strategy powered by small organic molecules are summarized.
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