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Dihydrogen Reduction of Carboxylic Esters to Alcohols under the Catalysis of Homogeneous Ruthenium Complexes: High Efficiency and Unprecedented Chemoselectivity
Abstract
The missing link: The presence of two N,P bridges in the ruthenium complexes used as catalysts for the title reaction is essential. Esters that contain isolated CC bonds are reduced to the corresponding unsaturated alcohols in high yields with high chemoselectivity (see example).
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Cited by
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Gunanathan, C., & Milstein, D. (2011) · Accounts of Chemical Research · doi:10.1021/ar2000265 · Cited by 1,078
Dub, P. A., & Ikariya, T. (2012) · ACS Catalysis · doi:10.1021/cs300341g · Cited by 386
Long-Chain Linear C 19 and C 23 Monomers and Polycondensates from Unsaturated Fatty Acid Esters
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Metadata
- Authors
- Saudan, L. A., Saudan, C. M., Debieux, C., & Wyss, P.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2007-09-20
- Volume
- 46
- Issue
- 39
- Pages
- 7473-7476
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2114216497
- Cited by
- 251
- References
- 0
- FWCI
- 3.42
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Dihydrogen Reduction of Carboxylic Esters to Alcohols under the Catalysis of Homogeneous Ruthenium Complexes: High Efficiency and Unprecedented Chemoselectivity. https://app.cochat.ai/papers/10.1002/anie.200701015
- The paper
- Saudan, L. A., Saudan, C. M., Debieux, C., & Wyss, P. (2007). Dihydrogen Reduction of Carboxylic Esters to Alcohols under the Catalysis of Homogeneous Ruthenium Complexes: High Efficiency and Unprecedented Chemoselectivity. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200701015
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