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Organocatalysis Mediated by (Thio)urea Derivatives
Abstract
Over the last decade the potential for N,N‐dialkyl(thio)urea derivatives to serve as active metal‐free organocatalysts for a wide range of synthetically useful reactions susceptible to the influence of general acid catalysis has begun to be realised. This article charts the development of these catalysts (with emphasis on the design principles involved), from early “proof‐of‐concept” materials to contemporary active chiral (bifunctional) promoters of highly selective asymmetric transformations.
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Cited by
Organocatalytic Ring-Opening Polymerization
Kamber, N. E., Jeong, W., Waymouth, R. M., Pratt, R. C., Lohmeijer, B. G. G., & Hedrick, J. L. (2007) · Chemical Reviews · doi:10.1021/cr068415b · Cited by 1,489
Asymmetric Aminocatalysis—Gold Rush in Organic Chemistry
Melchiorre, P., Marigo, M., Carlone, A., & Bartoli, G. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200705523 · Cited by 1,256
Asymmetric Organocatalysis: From Infancy to Adolescence
Dondoni, A., & Massi, A. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200704684 · Cited by 1,252
Organocatalytic Carbon–Sulfur Bond-Forming Reactions
Chauhan, P., Mahajan, S., & Enders, D. (2014) · Chemical Reviews · doi:10.1021/cr500235v · Cited by 632
Asymmetrische Organokatalyse: Eintritt in die Reifezeit
Dondoni, A., & Massi, A. (2008) · Angewandte Chemie · doi:10.1002/ange.200704684 · Cited by 398
Metadata
- Authors
- Connon, S. J.
- Venue
- Chemistry – A European Journal
- Publisher
- Wiley
- Published
- 2006-07-07
- Volume
- 12
- Issue
- 21
- Pages
- 5418-5427
- ISSN
- 0947-6539 (ISSN-L)
- 1521-3765
- OpenAlex
- W2075711137
- Cited by
- 846
- References
- 0
- FWCI
- 37.09
- Type
- journal article
- Language
- en
- Open access
- closed
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