The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Facile Conversion of Alcohols into Esters and Dihydrogen Catalyzed by New Ruthenium Complexes
Abstract
An efficient, environmentally benign method for the preparation of esters from alcohols under mild, neutral conditions without the need for carboxylic acid derivatives and condensing agents was developed. Catalyst design, based on new Ru(II) hydrido carbonyl complexes incorporating electron-rich PNP and PNN ligands has resulted in the novel complex (I) which is an outstanding catalyst for the dehydrogenation of primary alcohols to esters and H(2) under neutral conditions.
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Cites
Handbook of Heterogeneous Catalysis
(1997) · Wiley eBooks · doi:10.1002/9783527619474 · Cited by 2,387
Direct Condensation of Carboxylic Acids with Alcohols Catalyzed by Hafnium(IV) Salts
Ishihara, K., Ohara, S., & Yamamoto, H. (2000) · Science · doi:10.1126/science.290.5494.1140 · Cited by 336
Ruthenium-catalyzed oxidative transformation of alcohols and aldehydes to esters and lactones
Murahashi, S., Naota, T., Ito, K., Maeda, Y., & Taki, H. (1987) · The Journal of Organic Chemistry · doi:10.1021/jo00228a032 · Cited by 316
A convenient lactonization of diols to γ- and δ-lactones catalysed by transition metal polyhydrides
Lin, Y., Zhu, X., & Zhou, Y. (1992) · Journal of Organometallic Chemistry · doi:10.1016/0022-328x(92)83257-i · Cited by 68
Cited by
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Gunanathan, C., & Milstein, D. (2013) · Science · doi:10.1126/science.1229712 · Cited by 1,542
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Gunanathan, C., Ben-David, Y., & Milstein, D. (2007) · Science · doi:10.1126/science.1145295 · Cited by 1,288
Self-citationKhusnutdinova, J. R., & Milstein, D. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201503873 · Cited by 1,239
Self-citationGunanathan, C., & Milstein, D. (2011) · Accounts of Chemical Research · doi:10.1021/ar2000265 · Cited by 1,078
Self-citationRedox-active ligands in catalysis
Luca, O. R., & Crabtree, R. H. (2013) · Chem. Soc. Rev. · doi:10.1039/c2cs35228a · Cited by 1,039
Bond Activation and Catalysis by Ruthenium Pincer Complexes
Gunanathan, C., & Milstein, D. (2014) · Chemical Reviews · doi:10.1021/cr5002782 · Cited by 958
Self-citationSambVca 2. A Web Tool for Analyzing Catalytic Pockets with Topographic Steric Maps
Falivene, L., Credendino, R., Poater, A., Petta, A., Serra, L., Oliva, R., Scarano, V., & Cavallo, L. (2016) · Organometallics · doi:10.1021/acs.organomet.6b00371 · Cited by 907
Mellmann, D., Sponholz, P., Junge, H., & Beller, M. (2016) · Chemical Society Reviews · doi:10.1039/c5cs00618j · Cited by 872
Bis(imino)pyridines: Surprisingly Reactive Ligands and a Gateway to New Families of Catalysts
Gibson, V. C., Redshaw, C., & Solan, G. A. (2007) · Chemical Reviews · doi:10.1021/cr068437y · Cited by 845
Balaraman, E., Gunanathan, C., Zhang, J., Shimon, L. J. W., & Milstein, D. (2011) · Nature Chemistry · doi:10.1038/nchem.1089 · Cited by 655
Self-citationEfficient Homogeneous Catalytic Hydrogenation of Esters to Alcohols
Zhang, J., Leitus, G., Ben‐David, Y., & Milstein, D. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200503771 · Cited by 566
Self-citationHydrogen storage: beyond conventional methods
Dalebrook, A. F., Gan, W., Grasemann, M., Moret, S., & Laurenczy, G. (2013) · Chemical Communications · doi:10.1039/c3cc43836h · Cited by 503
A homogeneous transition metal complex for clean hydrogen production from methanol–water mixtures
Rodríguez-Lugo, R. E., Trincado, M., Vogt, M., Tewes, F., Santiso-Quinones, G., & Grützmacher, H. (2013) · Nature Chemistry · doi:10.1038/nchem.1595 · Cited by 416
Stempfle, F., Ortmann, P., & Mecking, S. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00705 · Cited by 397
Werkmeister, S., Neumann, J., Junge, K., & Beller, M. (2015) · Chemistry – A European Journal · doi:10.1002/chem.201500937 · Cited by 379
Efficient Hydrogenation of Ketones Catalyzed by an Iron Pincer Complex
Langer, R., Leitus, G., Ben‐David, Y., & Milstein, D. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201007406 · Cited by 375
Self-citationChemoselectivity and the Curious Reactivity Preferences of Functional Groups
Afagh, N. A., & Yudin, A. K. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200901317 · Cited by 320
Staubitz, A., Sloan, M. E., Robertson, A. P. M., Friedrich, A., Schneider, S., Gates, P. J., Schmedt auf der Günne, J., & Manners, I. (2010) · Journal of the American Chemical Society · doi:10.1021/ja104607y · Cited by 302
Nielsen, M., Junge, H., Kammer, A., & Beller, M. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201200625 · Cited by 293
Nguyen, D. H., Trivelli, X., Capet, F., Paul, J.-F., Dumeignil, F., & Gauvin, R. M. (2017) · ACS Catalysis · doi:10.1021/acscatal.6b03554 · Cited by 265
Krall, E. M., Klein, T. W., Andersen, R. J., Nett, A. J., Glasgow, R. W., Reader, D. S., Dauphinais, B. C., Mc Ilrath, S. P., Fischer, A. A., Carney, M. J., et al. (2014) · Chemical Communications · doi:10.1039/c4cc00541d · Cited by 224
Synthesis of High Molecular Weight Polyesters via In Vacuo Dehydrogenation Polymerization of Diols
Hunsicker, D. M., Dauphinais, B. C., Mc Ilrath, S. P., & Robertson, N. J. (2012) · Macromolecular Rapid Communications · doi:10.1002/marc.201100653 · Cited by 63
Metadata
- Authors
- Zhang, J., Leitus, G., Ben-David, Y., & Milstein, D.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2005-07-13
- Volume
- 127
- Issue
- 31
- Pages
- 10840-10841
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2050592102
- Cited by
- 803
- References
- 4
- FWCI
- 10.19
- Type
- journal article
- Language
- en
- Open access
- closed
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