Extending NHC-Catalysis: Coupling Aldehydes with Unconventional Reaction Partners

Biju, Akkattu T. ; Kuhl, Nadine ; Glorius, Frank (2011) Extending NHC-Catalysis: Coupling Aldehydes with Unconventional Reaction Partners Accounts of Chemical Research, 44 (11). pp. 1182-1195. ISSN 0001-4842

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Official URL: http://doi.org/10.1021/ar2000716

Related URL: http://dx.doi.org/10.1021/ar2000716

Abstract

Transition metal catalysis is a powerful means of effecting organic reactions, but it has some inherent drawbacks, such as the cost of the catalyst and the toxicity of the metals. Organocatalysis represents an attractive alternative and, in some cases, offers transformations unparalleled in metal catalysis. Unique transformations are a particular hallmark of N-heterocyclic carbene (NHC) organocatalysis, a versatile method for which a number of modes of action are known. The NHC-catalyzed umpolung (that is, the inversion of polarity) of electrophilic aldehydes, through formation of the nucleophilic Breslow intermediate, is probably the most important mode of action. In this Account, we discuss the reaction of Breslow intermediates with unconventional reaction partners.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society
ID Code:128728
Deposited On:03 Nov 2022 06:56
Last Modified:03 Nov 2022 06:56

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