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Journal articles on the topic 'Wilkinson’s Catalyst'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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1

Albayer, Mohammad, and Jason L. Dutton. "Reactions of Trivalent Iodine Reagents with Classic Iridium and Rhodium Complexes." Australian Journal of Chemistry 70, no. 11 (2017): 1180. http://dx.doi.org/10.1071/ch17173.

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In this work, the reactions of iodine(iii) reagents (PhI(L)2: L = pyridine, acetate (OAc−), triflate (OTf−)) with iridium(i) and rhodium(i) complexes (Vaskas’s compound, Wilkinson’s catalyst, and bis[bis(diphenylphosphino)ethane]rhodium(i) triflate) are reported. In all cases, the reactions resulted in two-electron oxidation of the metal complexes. Mixtures of products were observed in the reactions of Iiii reagents with Vaska’s compound and Wilkinson’s catalyst via ligand exchange and anion scrambling. In the case of reacting Iiii reagents with chelating ligand-containing bis[bis(diphenylphosphino)ethane]rhodium(i) triflate, no scrambling was observed.

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2

Osei Akoto, Clement, and Jon D. Rainier. "Concise Seven-Membered Oxepene/Oxepane Synthesis – Structural Motifs in Natural and Synthetic Products." Synthesis 51, no. 18 (May 20, 2019): 3529–35. http://dx.doi.org/10.1055/s-0037-1611838.

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This work outlines a suitable method for the synthesis of oxepane skeleton using iterative C-glycoside technology on the oxepene intermediate, which was synthesized utilizing Wilkinson’s catalyst [Rh(PPh3)3Cl] to generate the isomerized product in a linear synthetic manner. The central core of the oxepene motif was achieved via an olefin metathesis reaction using the Grubbs second-generation and Schrock catalysts. The synthesis of the functionalized oxepane having the desired adriatoxin E-ring relative stereochemistry was achieved starting from commercially available homopropargylic alcohol.

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3

Kyselka, J., L. Thomes, S. Remišová, M. Dragoun, M. Berčíková, and V. Filip. "Preparation of conjugated linoleic acid enriched derivatives by conventional and biphasic isomerisation." Czech Journal of Food Sciences 34, No. 6 (December 21, 2016): 511–21. http://dx.doi.org/10.17221/362/2016-cjfs.

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The preparation of conjugated linoleic acid (CLA)-enriched free fatty acids by industrial processes compared with our biphasic isomerisation experiments in a special designed reactor enabling the preparation of CLA esters was evaluated. Our experiments further revealed the main disadvantage of semi-synthetic alkali isomerisation to be the formation of conjugated E,E-octadecadienoic acid isomers (2.92–3.44%) and the bioavailability of free fatty acid products. Urea fractionation technology improved the quality of the reaction mixture, but at the same time the yield of rumenic acid was decreased on purification. Therefore, we decided to apply complexes of noble metals in order to isomerise linoleic acid ester derivatives. The known Wilkinson’s hydrogenation catalyst, RhCl (PPh<sub>3</sub>)<sub>3</sub>, was found to be the most effective. We investigated the preparation of bioavailable CLA-enriched triacylglycerols. Special attention was paid to recycling of Wilkinson’s catalyst.

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4

Patel, Pranav, Chih-Tsung Chang, Namin Kang, Gue-Jae Lee, William S. Powell, and Joshua Rokach. "Reductive deprotection of silyl groups with Wilkinson’s catalyst/catechol borane." Tetrahedron Letters 48, no. 30 (July 2007): 5289–92. http://dx.doi.org/10.1016/j.tetlet.2007.05.118.

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5

Bezuidenhoudt, Barend, Johannes van Tonder, Charlene Marais, and David Cole-Hamilton. "Regioselective Hydrogenation of α,β-Unsaturated Ketones over Wilkinson’s Catalyst." Synthesis 2010, no. 03 (November 13, 2009): 421–24. http://dx.doi.org/10.1055/s-0029-1217117.

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6

Yang, Zhenyu, Maike H. Wahl, and Jonathan G. C. Veinot. "Size-independent organosilane functionalization of silicon nanocrystals using Wilkinson’s catalyst." Canadian Journal of Chemistry 92, no. 10 (October 2014): 951–57. http://dx.doi.org/10.1139/cjc-2014-0048.

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A low-temperature size-independent method for modifying the surface chemistry of the silicon nanocrystal (SiNC) surface is reported. Wilkinson’s catalyst has been applied to accelerate the dehydrogenative coupling reaction between organosilane molecules and hydride-terminated SiNCs. Two strategies and multiple organosilanes were evaluated to study surface modification efficiency. During the investigations, it was determined that surface functionalization efficiency showed some dependence upon the organic modifier in question. The comparatively low reactivity of octadecyldimethyl silanes may result from the formation of “Si–Rh–Si” intermediates hindered by the steric bulk of the silanes when reacted with activated SiNCs. Quenching of the SiNC-based photoluminescence is observed and the origin of this phenomenon has been attributed to the present of trace rhodium on SiNCs detected using X-ray photoelectron spectroscopy.

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7

Leitmannová, Eliška, Petr Jirásek, Jakub Rak, Lucie Potucká, Petr Kačer, and Libor Červený. "Terminal C≡C triple bond hydrogenation using immobilized Wilkinson’s catalyst." Research on Chemical Intermediates 36, no. 5 (September 2010): 511–22. http://dx.doi.org/10.1007/s11164-010-0162-1.

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8

Yang, Lijuan, Hui Wang, Garry L. Rempel, and Qinmin Pan. "Recovery of Wilkinson’s Catalyst from Hydrogenated Nitrile Butadiene Rubber Latex Nanoparticles." Topics in Catalysis 57, no. 17-20 (September 5, 2014): 1558–63. http://dx.doi.org/10.1007/s11244-014-0333-1.

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9

Kramer, Jurjen, Erica Nöllen, Wim Buijs, Willem L. Driessen, and Jan Reedijk. "Investigations into the recovery of Wilkinson’s catalyst with silica-immobilised P-donor ligands." Reactive and Functional Polymers 57, no. 1 (November 2003): 1–11. http://dx.doi.org/10.1016/j.reactfunctpolym.2003.06.001.

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10

Grünberg, Anna, Xu Yeping, Hergen Breitzke, and Gerd Buntkowsky. "Solid-State NMR Characterization of Wilkinson’s Catalyst Immobilized in Mesoporous SBA-3 Silica." Chemistry - A European Journal 16, no. 23 (May 5, 2010): 6993–98. http://dx.doi.org/10.1002/chem.200903322.

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11

Kim, Kwang Ho, Joon Weon Choi, Chang Soo Kim, and Keunhong Jeong. "Parahydrogen-induced polarization in the hydrogenation of lignin-derived phenols using Wilkinson’s catalyst." Fuel 255 (November 2019): 115845. http://dx.doi.org/10.1016/j.fuel.2019.115845.

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12

Bugoni, Serena, Debora Boccato, Alessio Porta, Giuseppe Zanoni, and Giovanni Vidari. "Enantioselective Divergent Synthesis of (−)-cis-α- and (−)-cis-γ-Irone by Using Wilkinson’s Catalyst." Chemistry - A European Journal 21, no. 2 (October 30, 2014): 791–99. http://dx.doi.org/10.1002/chem.201404642.

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13

Witulski, Bernhard, Thomas Stengel, and Jesús M. Fernández-Hernández. "Chemo- and regioselective crossed alkyne cyclotrimerisation of 1,6-diynes with terminal monoalkynes mediated by Grubbs’ catalyst or Wilkinson’s catalyst." Chemical Communications, no. 19 (2000): 1965–66. http://dx.doi.org/10.1039/b005636g.

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14

Srour, Mohamad, Sara Hadjiali, Kai Brunnengräber, Heiko Weidler, Yeping Xu, Hergen Breitzke, Torsten Gutmann, and Gerd Buntkowsky. "A Novel Wilkinson’s Type Silica Supported Polymer Catalyst: Insights from Solid-State NMR and Hyperpolarization Techniques." Journal of Physical Chemistry C 125, no. 13 (March 24, 2021): 7178–87. http://dx.doi.org/10.1021/acs.jpcc.1c00112.

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15

Qiu, Xiaodong, Hong Deng, Yue Zhao, and Zhuangzhi Shi. "Rhodium-catalyzed, P-directed selective C7 arylation of indoles." Science Advances 4, no. 12 (December 2018): eaau6468. http://dx.doi.org/10.1126/sciadv.aau6468.

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The indole scaffold will continue to play a vital role in the future of drug discovery and agrochemical development. Regioselective direct arylation of indoles on the benzenoid moiety is a challenging task due to the inherent reactivity of the C2 and C3 positions. Here, we have developed an effective strategy for the regioselective direct arylation of indoles at the C7 position with (hetero)aryl bromides by the rational design of a directing group. The key to the high selectivity and reactivity of this method is the appropriate selection of a class of directing groups, N-PR2(R =tBu andcHex), that are easily removed in the presence of the Wilkinson’s catalyst. Using the present method as a key step, formal synthesis of marine alkaloid dictyodendrin B has also been demonstrated.

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16

Abdulhussain, Safaa, Hergen Breitzke, Tomasz Ratajczyk, Anna Grünberg, Mohamad Srour, Danjela Arnaut, Heiko Weidler, et al. "Synthesis, Solid-State NMR Characterization, and Application for Hydrogenation Reactions of a Novel Wilkinson’s-Type Immobilized Catalyst." Chemistry - A European Journal 20, no. 4 (December 12, 2013): 1159–66. http://dx.doi.org/10.1002/chem.201303020.

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17

Dachs, Anna, Sílvia Osuna, Anna Roglans, and Miquel Solà. "Density Functional Study of the [2+2+2] Cyclotrimerization of Acetylene Catalyzed by Wilkinson’s Catalyst, RhCl(PPh3)3." Organometallics 29, no. 3 (February 8, 2010): 562–69. http://dx.doi.org/10.1021/om900836b.

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18

Choinopoulos, Ioannis, Ioannis Papageorgiou, Silverio Coco, Emmanuel Simandiras, and Spyros Koinis. "Modification of Wilkinson’s catalyst with triphenyl phosphite: Synthesis, structure, 31P NMR and DFT study of trans-[RhCl(P(OPh)3)(PPh3)2]." Polyhedron 45, no. 1 (September 2012): 255–61. http://dx.doi.org/10.1016/j.poly.2012.06.086.

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19

Matsubara, Toshiaki, Ryohei Takahashi, and Saori Asai. "ONIOM Study of the Mechanism of Olefin Hydrogenation by the Wilkinson’s Catalyst: Reaction Paths and Energy Surfaces of trans- and cis-Forms." Bulletin of the Chemical Society of Japan 86, no. 2 (February 15, 2013): 243–54. http://dx.doi.org/10.1246/bcsj.20120113.

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20

Goodman, Jenni, Vladimir V. Grushin, Roman B. Larichev, Stuart A. Macgregor, William J. Marshall, and D. Christopher Roe. "Fluxionality of [(Ph3P)3M(X)] (M = Rh, Ir). The Red and Orange Forms of [(Ph3P)3Ir(Cl)]. Which Phosphine Dissociates Faster from Wilkinson’s Catalyst?" Journal of the American Chemical Society 132, no. 34 (September 2010): 12013–26. http://dx.doi.org/10.1021/ja1039693.

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21

Panagiotopoulos, Athanassios A., Efthymios G. Fasoulakis, Eleftheria E. Vardalachaki, and Athanassios G. Coutsolelos. "Photocatalytic hydrogen production based on a water-soluble porphyrin derivative as sensitizer and a series of Wilkinson type complexes as catalysts." Journal of Porphyrins and Phthalocyanines 20, no. 08n11 (August 2016): 1200–1206. http://dx.doi.org/10.1142/s1088424616500905.

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Herein, we report photochemical hydrogen evolution systems consisting of various rhodium based catalysts with Wilkinson type structures, Zn metalated porphyrins and fluorescein as photosensitizers and triethanolamine as a sacrificial electron donor in acetonitrile/H2O (1:1) solution. Since rhodium complexes 1 and 2 are used for the first time as catalysts in this type of systems, a systematic study was performed in order to elucidate the best conditions for H2 production. Upon visible irradiation hydrogen production was detected and the best results were obtained at pH 7 when dye P3 and catalyst 1 were used with a TON of 61, after 48 h and in the presence of dye P1 and catalyst 2 with a TON of 69, after the 48 h.

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22

McManus, N. T., and G. L. Rempel. "Improvements in the Hydrogenation of Nitrile Rubber Using Wilkinson's Catalyst." Rubber Chemistry and Technology 81, no. 2 (May 1, 2008): 227–43. http://dx.doi.org/10.5254/1.3548207.

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Abstract RhCl(PPh3)3 is an efficient catalyst precursor for the selective hydrogenation of C=C in acrylonitrile butadiene rubber(“nitrile rubber”, NBR). The established technology for the process using RhCl(PPh3)3 is to carry out reaction in the presence of a large excess of triphenylphosphine (PPh3), with monochlorobenzene (MCB) as solvent. In parallel with the hydrogenation of unsaturation in the rubber there is a side reaction involving the MCB, which produces benzene. This likely occurs via oxidative addition of the C-Cl bond in the monochlorobenzene to a Rh intermediate in the catalytic cycle for hydrogenation, followed by reductive elimination of benzene in conjunction with H2 addition to the Rh centre. This leads to formation of less active Rh intermediates which lead to rapid deterioration of catalytic activity in the absence of excess PPh3. It was postulated that some of the PPh3 in solution acts as a base that “mops up” excess HCl formed as a by product of the catalytic cycle. Supporting evidence comes from a novel improvement of the hydrogenation process, where the deactivation of catalyst, can be offset by the presence of bases, such as amines and metal oxides (as an alternative to adding a large excess of PPh3). This modification can improve catalyst activity with respect to levels of Rh used, or could be used to minimize the level of added co-catalysts needed to maintain useful rates of hydrogenation.

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23

Tanielyan, Setrak K., Robert L. Augustine, Norman Marin, and Gabriela Alvez. "Anchored Wilkinson Catalyst." ACS Catalysis 1, no. 2 (January 21, 2011): 159–69. http://dx.doi.org/10.1021/cs100069f.

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24

Schumacher, Christian, Deborah E. Crawford, Branimir Raguž, Robert Glaum, Stuart L. James, Carsten Bolm, and José G. Hernández. "Mechanochemical dehydrocoupling of dimethylamine borane and hydrogenation reactions using Wilkinson's catalyst." Chemical Communications 54, no. 60 (2018): 8355–58. http://dx.doi.org/10.1039/c8cc04487b.

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25

Martinez, Araceli, Mikhail A. Tlenkopatchev, and Selena Gutierrez. "The Unsaturated Polyester Via Ring-Opening Metathesis Polymerization (ROMP) of ω-6-Hexadecenlactone." Current Organic Synthesis 15, no. 4 (June 12, 2018): 566–71. http://dx.doi.org/10.2174/1570179414666171011155831.

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Background: Ring opening metathesis polymerization of lactones using alkylidene catalysts is an alternative to obtain unsaturated linear polyesters with remarkable thermal and mechanical properties. Also, these polyesters have properties of biodegradability which opens up a wide range of applications as environmentally friendly thermoplastics and biomaterials. Objective: This research aims to present one route to obtain an unsaturated linear polyester poly(ω-6- hexadecenlactone) via ring opening-metathesis polymerization of ω-6-hexadecenlactone using the rutheniumalkylidene [Ru(Cl)2(=CHPh)(PCy3)2] (I), [Ru(Cl2)(=CHPh)(1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)( PCy3)] (II) and [Ru(Cl2)(=CH(o-isopropoxyphenylmethylene))(1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)] (III) and the ruthenium-vinylidene [RuCl2(=C=CH(p-C6H4CF3))(PCy3)2] (IV) catalysts. Conclusion: The high number-average molecular weights of the poly(ω-6-hexadecenlactone) between Mn = 114,800-155,400 g/mol and yields ranging from 96 to 98 % can be achieved by II and III catalysts. The catalysts II and III with the N-heterocyclic carbene ligand showed superior activity and stability upon catalysts I and IV bearing PCy3 ligands. The hydrogenation of poly(ω-6-hexadecenlactone) using Wilkinson catalyst [RhCl(PPh3)3] was studied. The percent crystallinity of the unsaturated poly(ω-6-hexadecenlactone) was 31% with a melting temperature 47.60ºC. Stress-strain measurements of several poly(ω-6-hexadecenlactone) were determined.

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26

Shoai, Shiva, Paul Bichler, Baldip Kang, Heather Buckley, and Jennifer A. Love. "Catalytic Alkyne Hydrothiolation with Alkanethiols using Wilkinson's Catalyst." Organometallics 26, no. 24 (November 2007): 5778–81. http://dx.doi.org/10.1021/om700811e.

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27

Mikaya, A. I., V. G. Zaikin, and V. M. Vdovin. "Gas-phase deuteration of olefins over Wilkinson's catalyst." Journal of Molecular Catalysis 32, no. 3 (August 1985): 353–55. http://dx.doi.org/10.1016/0304-5102(85)85088-4.

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28

Brinkman, Herbert R., William H. Miles, Michael D. Hilborn, and Michael C. Smith. "The Reduction of Nitrobenzenes by Triethylsilane Using Wilkinson's Catalyst." Synthetic Communications 26, no. 5 (March 1996): 973–80. http://dx.doi.org/10.1080/00397919608003701.

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29

Parent, Alexander R., James D. Blakemore, Gary W. Brudvig, and Robert H. Crabtree. "Wilkinson's iridium acetate trimer as a water-oxidation catalyst." Chemical Communications 47, no. 42 (2011): 11745. http://dx.doi.org/10.1039/c1cc15501f.

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30

Rosenberg, Lisa, Colin W. Davis, and Junzhi Yao. "Catalytic Dehydrogenative Coupling of Secondary Silanes Using Wilkinson's Catalyst." Journal of the American Chemical Society 123, no. 21 (May 2001): 5120–21. http://dx.doi.org/10.1021/ja015697i.

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31

Rosenberg, Lisa, and Danielle N. Kobus. "Dehydrogenative coupling of primary alkyl silanes using Wilkinson's catalyst." Journal of Organometallic Chemistry 685, no. 1-2 (November 2003): 107–12. http://dx.doi.org/10.1016/s0022-328x(03)00712-5.

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32

Pal, Indrani, Swati Dutta, Falguni Basuli, Savitha Goverdhan, Shie-Ming Peng, Gene-Hsiang Lee, and Samaresh Bhattacharya. "Unprecedented Chemical Transformation of Semicarbazones Mediated by Wilkinson's Catalyst." Inorganic Chemistry 42, no. 14 (July 2003): 4338–45. http://dx.doi.org/10.1021/ic034247j.

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33

Azpeitia, Susan, Belén Fernández, María A. Garralda, and Miguel A. Huertos. "Dehydrogenative Coupling of a Tertiary Silane Using Wilkinson's Catalyst." European Journal of Inorganic Chemistry 2016, no. 18 (June 2016): 2891–95. http://dx.doi.org/10.1002/ejic.201600395.

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34

Azpeitia, Susan, Belén Fernández, María A. Garralda, and Miguel A. Huertos. "Dehydrogenative Coupling of a Tertiary Silane Using Wilkinson's Catalyst." European Journal of Inorganic Chemistry 2016, no. 18 (June 2016): 2863. http://dx.doi.org/10.1002/ejic.201600672.

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35

Tanielyan, Setrak, Nicole Biunno, Ramesh Bhagat, and Robert Augustine. "Anchored Wilkinson Catalyst: Hydrogenation of β Pinene." Topics in Catalysis 57, no. 17-20 (September 3, 2014): 1564–69. http://dx.doi.org/10.1007/s11244-014-0332-2.

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36

Hill, Richard K., Claudio Abächerli, and Sanji Hagishita. "Synthesis of (2S,4S)- and (2S,4R)-[5,5,5-2H3] leucine from (R)-pulegone." Canadian Journal of Chemistry 72, no. 1 (January 1, 1994): 110–13. http://dx.doi.org/10.1139/v94-017.

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Beginning with (R)-pulegone, a CD3 group attached to the stereogenic center containing CH3 has been created by conversion to citronellal-1-d, exchange of the acidic hydrogens at C-2 by deuterium, and decarbonylation with Wilkinson's catalyst. Oxidation to isovaleric acid-d3 and conversion to leucine by standard procedures gave the (2S,4S) and (2R,4S) diastereomers (10 and 12) of [5,5,5-2H3]leucine.

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37

Evans, P. Andrew, and Jade D. Nelson. "Regioselective rhodium-catalyzed allylic alkylation with a modified Wilkinson's catalyst." Tetrahedron Letters 39, no. 13 (March 1998): 1725–28. http://dx.doi.org/10.1016/s0040-4039(98)00142-7.

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38

Quiroga, M. E., E. A. Cagnola, D. A. Liprandi, and P. C. L'Argentière. "Supported Wilkinson's complex used as a high active hydrogenation catalyst." Journal of Molecular Catalysis A: Chemical 149, no. 1-2 (December 1999): 147–52. http://dx.doi.org/10.1016/s1381-1169(99)00164-8.

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39

Li, P., and S. Kawi. "Dendritic SBA-15 supported Wilkinson's catalyst for hydroformylation of styrene." Catalysis Today 131, no. 1-4 (February 2008): 61–69. http://dx.doi.org/10.1016/j.cattod.2007.10.090.

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40

BAUER, R., and H. WERNER. "Investigations on a homogeneous wilkinson's catalyst for the water photolysis." International Journal of Hydrogen Energy 19, no. 6 (June 1994): 497–99. http://dx.doi.org/10.1016/0360-3199(94)90003-5.

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41

Grushin, Vladimir V., and William J. Marshall. "The Fluoro Analogue of Wilkinson's Catalyst and Unexpected Ph−Cl Activation†." Journal of the American Chemical Society 126, no. 10 (March 2004): 3068–69. http://dx.doi.org/10.1021/ja049844z.

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42

Perea-Buceta, Jesus E., Israel Fernández, Sami Heikkinen, Kirill Axenov, Alistair W. T. King, Teemu Niemi, Martin Nieger, Markku Leskelä, and Timo Repo. "Diverting Hydrogenations with Wilkinson's Catalyst towards Highly Reactive Rhodium(I) Species." Angewandte Chemie 127, no. 48 (October 6, 2015): 14529–33. http://dx.doi.org/10.1002/ange.201506216.

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43

Perea-Buceta, Jesus E., Israel Fernández, Sami Heikkinen, Kirill Axenov, Alistair W. T. King, Teemu Niemi, Martin Nieger, Markku Leskelä, and Timo Repo. "Diverting Hydrogenations with Wilkinson's Catalyst towards Highly Reactive Rhodium(I) Species." Angewandte Chemie International Edition 54, no. 48 (October 6, 2015): 14321–25. http://dx.doi.org/10.1002/anie.201506216.

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44

Nejat, Razieh, and Alireza Mahjoub. "Magnetically water-dispersible and recoverable rhodium organometallic catalyst derived from Wilkinson's catalyst for promoting organic reactions." Applied Organometallic Chemistry 31, no. 7 (November 10, 2016): e3657. http://dx.doi.org/10.1002/aoc.3657.

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45

Singha, Nikhil K., S. Sivaram, and S. S. Talwar. "A New Method to Hydrogenate Nitrile Rubber in the Latex Form." Rubber Chemistry and Technology 68, no. 2 (May 1, 1995): 281–86. http://dx.doi.org/10.5254/1.3538742.

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Abstract A water soluble analog of Wilkinson catalyst — chloro-tris-(sodium diphenylphosphino-benzene-m-sulfonate) rhodium(I), CAS 67178-14-7, i.e. RhCl(DPM)3— has been found to hydrogenate NBR latex. More than 60 mol% hydrogenation can be achieved at 75°C and 1 atmosphere hydrogen pressure. Hydrogenation was accompanied by an increase in gel content of the latex.

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46

Singha, Nikhil K., S. S. Talwar, and S. Sivaram. "Solution Hydrogenation of Chloroprene Rubber Using a Wilkinson Catalyst." Macromolecules 27, no. 23 (November 1994): 6985–87. http://dx.doi.org/10.1021/ma00101a041.

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47

Li, Peng, Warintorn Thitsartarn, and Sibudjing Kawi. "Highly Active and Selective Nanoalumina-Supported Wilkinson’s Catalysts for Hydroformylation of Styrene." Industrial & Engineering Chemistry Research 48, no. 4 (February 18, 2009): 1824–30. http://dx.doi.org/10.1021/ie800715k.

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48

Thalji, R. K., K. A. Ahrendt, R. G. Bergman, and J. A. Ellman. "Annulation of Aromatic Imines via Directed C−H Activation with Wilkinson's Catalyst." Journal of the American Chemical Society 123, no. 39 (October 2001): 9692–93. http://dx.doi.org/10.1021/ja016642j.

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49

Wei, Zhenli, Jialong Wu, Qinmin Pan, and Garry L. Rempel. "Direct Catalytic Hydrogenation of an Acrylonitrile-Butadiene Rubber Latex Using Wilkinson's Catalyst." Macromolecular Rapid Communications 26, no. 22 (November 14, 2005): 1768–72. http://dx.doi.org/10.1002/marc.200500553.

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50

Zhang, Mingbao, Lei Zhu, Xin Ma, Miao Dai, and Derek Lowe. "Carboxylate-Directed Highly Stereoselective Homogeneous Hydrogenation of Cyclic Olefins with Wilkinson's Catalyst." Organic Letters 5, no. 9 (May 2003): 1587–89. http://dx.doi.org/10.1021/ol034464o.

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