Efficient reactions in aqueous organic chemistry do not require soluble reactants, as had been thought. A newly developed ‘on-water’ protocol is characterized by short reaction times, and the products are easy to isolate.
References
Daniel, R. M., Finney, J. L. & Stoneham, M. (eds) Phil. Trans. R. Soc. Lond. B 359, 1141–1328 (2004).
Narayan, S. et al. Angew. Chem. Int. Edn 44, 3275–3279 (2005).
Breslow, R. & Rideout, D. C. J. Am. Chem. Soc. 102, 7816–7817 (1980).
Grieco, P. A. (ed.) Organic Synthesis in Water (Blackie, London, 1998).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Klijn, J., Engberts, J. Fast reactions ‘on water’. Nature 435, 746–747 (2005). https://doi.org/10.1038/435746a
Published:
Issue Date:
DOI: https://doi.org/10.1038/435746a
- Springer Nature Limited
This article is cited by
-
Unified picture of vibrational relaxation of OH stretch at the air/water interface
Nature Communications (2024)
-
Step-Wise, Tandem One-Pot Syntheses and Antifungal Evaluation of 2-(4-oxo-3,4-dihydroquinazolin-2-yl)-N-arylbenzamides in Water – a Green Protocol
Pharmaceutical Chemistry Journal (2024)
-
The photochemical reaction of phenol becomes ultrafast at the air–water interface
Nature Chemistry (2021)
-
A facile and efficient method for the synthesis of crystalline tetrahydro-β-carbolines via the Pictet-Spengler reaction in water
Scientific Reports (2020)
-
Green synthesis, antitubercular evaluation, and molecular docking studies of ethyl 3,5-dicyano-6-oxo-2,4-diarylpiperidine-3-carboxylate derivatives
Medicinal Chemistry Research (2020)