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RANEY® Ni catalyzed transfer hydrogenation of levulinate esters to γ-valerolactone at room temperature
Abstract
A catalytic transfer hydrogenation process was developed for the production of γ-valerolactone (GVL) from ethyl levulinate (EL) and a H-donor at room temperature. Ethyl levulinate was almost quantitatively converted to γ-valerolactone. Further, a two step process for producing GVL from biomass derived platform molecules was also reported.
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Citations
Cites
Chemical Routes for the Transformation of Biomass into Chemicals
Corma, A., Iborra, S., & Velty, A. (2007) · Chemical Reviews · doi:10.1021/cr050989d · Cited by 5,970
Metal Chlorides in Ionic Liquid Solvents Convert Sugars to 5-Hydroxymethylfurfural
Zhao, H., Holladay, J. E., Brown, H., & Zhang, Z. C. (2007) · Science · doi:10.1126/science.1141199 · Cited by 1,997
Cited by
Song, J., Zhou, B., Zhou, H., Wu, L., Meng, Q., Liu, Z., & Han, B. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201504001 · Cited by 289
Influence of solvent structure and hydrogen bonding on catalysis at solid–liquid interfaces
Potts, D. S., Bregante, D. T., Adams, J. S., Torres, C., & Flaherty, D. W. (2021) · Chemical Society Reviews · doi:10.1039/d1cs00539a · Cited by 190
Metadata
- Authors
- Yang, Z., Huang, Y.-B., Guo, Q.-X., & Fu, Y.
- Venue
- Chemical Communications
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2013
- Volume
- 49
- Issue
- 46
- Pages
- 5328
- ISSN
- 1359-7345 (ISSN-L)
- 1364-548X
- OpenAlex
- W2068205996
- Cited by
- 209
- References
- 2
- FWCI
- 10.98
- Type
- journal article
- Language
- en
- Open access
- closed
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- Yang, Z., Huang, Y.-B., Guo, Q.-X., & Fu, Y. (2013). RANEY® Ni catalyzed transfer hydrogenation of levulinate esters to γ-valerolactone at room temperature. Chemical Communications. https://doi.org/10.1039/c3cc40980e
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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
