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Journal articles on the topic 'Au-catalyzed'

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Author: Grafiati

Published: 11 March 2023

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1

Pung, Swee Yong, Chee Chee Tee, Kwang Leong Choy, and Xiang Hui Hou. "Growth Mechanism of Au-Catalyzed Zno Nanowires: VLS or VS-VLS?" Advanced Materials Research 364 (October 2011): 333–37. http://dx.doi.org/10.4028/www.scientific.net/amr.364.333.

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A systematic study was carried out to study the effect of process parameters on the growth of Au-catalyzed ZnO nanowires (NWs). Growth of Au-catalyzed ZnO NWs could be mainly occurred at the tip or at the base of NWs. This study provided useful information in determining the process window for the tip-growth Au-catalyzed ZnO NWs. Besides, a generic growth mechanism, i.e. a combination of Vapor-Liquid-Solid and Vapor-Solid (VLS and VS) mechanism is proposed to explain the tip-growth and base-growth Au-catalyzed ZnO NWs.

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2

Rodriguez, Jessica, Nicolas Adet, Nathalie Saffon-Merceron, and Didier Bourissou. "Au(i)/Au(iii)-Catalyzed C–N coupling." Chemical Communications 56, no. 1 (2020): 94–97. http://dx.doi.org/10.1039/c9cc07666b.

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3

Reeves, Ryan D., Caitlin N. Kinkema, Eleanor M. Landwehr, Logan E. Vine, and Jennifer M. Schomaker. "Stereodivergent Metal-Catalyzed Allene Cycloisomerizations." Synlett 31, no. 06 (February 4, 2020): 627–31. http://dx.doi.org/10.1055/s-0037-1610746.

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Metal-catalyzed allene cycloisomerizations provide rapid entry into five-membered carbocyclic frameworks, a common motif in natural products and pharmaceuticals. While both Au(I) and Pd(0)-catalyzed allene cycloisomerizations give 5-endo-dig cyclization, Pd prefers the syn diastereomer in contrast to the anti isomer observed with Au. The change in stereoselectivity is proposed to arise from buildup of A1,3 strain during the key carbopalladation step to furnish the cycloisomerized products in moderate to good dr with yields comparable to Au(I) catalysts.

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4

Shi, Min, and Qiang Wang. "Synthesis of Cyclic and Heterocyclic Compounds via Gold-Catalyzed Reactions." Synlett 28, no. 17 (July 27, 2017): 2230–40. http://dx.doi.org/10.1055/s-0036-1590827.

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This account outlines the latest advances from our group in the field of gold catalysis. A variety of cyclic and heterocyclic compounds, containing different sized skeletons, are synthesized selectively by fine-tuning the substrates, catalysts, and ligands. Au(I)/Au(III) redox catalysis is applied in our latest work through adding external oxidation. The reaction mechanisms are discussed in detail. Moreover, the photoredox catalytic process is also introduced briefly, which opens avenues for the development of new strategies in gold chemistry.1 Introduction2 Gold-Catalyzed Cycloisomerization of Enynes3 Gold-Catalyzed Intramolecular Cyclization of Propargylic Ester Substrates4 Gold-Catalyzed C(sp3)–H Functionalizations5 The Au(I)/Au(III) Redox Catalytic Cycle6 Conclusion

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5

Лещенко, Е. Д., and В. Г. Дубровский. "Моделирование профиля состава осевой гетероструктуры InSb/GaInSb/InSb в нитевидных нанокристаллах." Письма в журнал технической физики 48, no. 19 (2022): 20. http://dx.doi.org/10.21883/pjtf.2022.19.53590.19339.

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The formation of the double InSb/GaInSb/InSb heterostructure in self-catalyzed and Au-catalyzed nanowires is studied theoretically. We calculate the compositional profiles across the axial heterostructures and study the influence of different growth parameters on the heterointerface properties, including temperature, Sb and Au concentrations.

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6

Leshchenko E. D. and Dubrovskii V. G. "Modeling the compositional profiles across axial InSb/GaInSb/InSb nanowire heterostructures." Technical Physics Letters 48, no. 10 (2022): 17. http://dx.doi.org/10.21883/tpl.2022.10.54790.19339.

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The formation of the double InSb/GaInSb/InSb heterostructure in self-catalyzed and Au-catalyzed nanowires is studied theoretically. We calculate the compositional profiles across the axial heterostructures and study the influence of different growth parameters on the heterointerface properties, including temperature, Sb and Au concentrations. Keywords: III-V nanowires, axial heterostructure, heterointerface, modeling

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7

Bhunia, Sabyasachi, and Rai-Shung Liu. "Access to molecular complexity via gold- and platinum-catalyzed cascade reactions." Pure and Applied Chemistry 84, no. 8 (March 31, 2012): 1749–57. http://dx.doi.org/10.1351/pac-con-11-09-13.

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We report recent progress on Au- and Pt-catalyzed cascade reactions to access complicated molecular frameworks. Reported reactions include new cyclization/cycloaddition cascades on carbonyl and epoxide substrates tethered with an allene, alkene, and alkyne. Such substrates enable Au-catalyzed cascade reactions comprising an initial cyclization to form reactive 1,n-dipole that undergoes subsequent cycloadditions with suitable dipolarophiles.

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8

Dubrovskii, V. G., N. V. Sibirev, Y. Berdnikov, U. P. Gomes, D. Ercolani, V. Zannier, and L. Sorba. "Length distributions of Au-catalyzed and In-catalyzed InAs nanowires." Nanotechnology 27, no. 37 (August 8, 2016): 375602. http://dx.doi.org/10.1088/0957-4484/27/37/375602.

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9

Xu, Shao Hong. "Au-Catalyzed Homocoupling of Terminal Alkynes." Applied Mechanics and Materials 184-185 (June 2012): 900–903. http://dx.doi.org/10.4028/www.scientific.net/amm.184-185.900.

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The homocoupling reaction of alkynes was carried out smoothly in the presence of 10 mol% AuCl3 using I2 as oxidant to generate diyned products in high yields. The method is simple, efficient, safe and AuClPh3 also showed comparable catalytic activity to this transformation.

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10

Aponick, Aaron, Chuan-Ying Li, and Berenger Biannic. "Au-Catalyzed Cyclization of Monoallylic Diols." Organic Letters 10, no. 4 (February 2008): 669–71. http://dx.doi.org/10.1021/ol703002p.

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11

Kanjanachuchai, Songphol, Thipusa Wongpinij, Chanan Euaruksakul, and Pat Photongkam. "Au-catalyzed desorption of GaAs oxides." Nanotechnology 30, no. 21 (March 15, 2019): 215703. http://dx.doi.org/10.1088/1361-6528/ab062e.

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12

Ho, Tam D., and Michael P. Schramm. "Au-Cavitand Catalyzed Alkyne-Acid Cyclizations." European Journal of Organic Chemistry 2019, no. 33 (August 12, 2019): 5678–84. http://dx.doi.org/10.1002/ejoc.201900829.

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13

García‐Fernández, Pedro D., Cristina Izquierdo, Javier Iglesias‐Sigüenza, Elena Díez, Rosario Fernández, and José M. Lassaletta. "Au I ‐Catalyzed Haloalkynylation of Alkenes." Chemistry – A European Journal 26, no. 3 (December 17, 2019): 629–33. http://dx.doi.org/10.1002/chem.201905078.

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14

Bhattacharjee, Debajyoti, Bhupesh Kumar Mishra, Arup Kumar Chakrabartty, and Ramesh Ch Deka. "Catalytic activity of anionic Au–Ag dimer for nitric oxide oxidation: a DFT study." New Journal of Chemistry 39, no. 3 (2015): 2209–16. http://dx.doi.org/10.1039/c4nj01328j.

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15

Kumar, Dhurjati Prasad. "Synthesis of gold nanoparticles and nanoclusters in a supramolecular gel and their applications in catalytic reduction of p-nitrophenol to p-aminophenol and Hg(ii) sensing." RSC Adv. 4, no. 85 (2014): 45449–57. http://dx.doi.org/10.1039/c4ra07532c.

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Seven gelator molecules giving supramolecular gels produced Au-nanoparticles and fluorescent, small Au-nanoclusters. Such Au-nanoparticle containing gels catalyzed the reduction of p-nitrophenol to p-aminophenol without NaBH₄. The fluorescent Au-nanoclusters acted as a Hg(ii) sensor.

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16

Kidonakis, Marios, and Manolis Stratakis. "Reduction of the Diazo Functionality of α-Diazocarbonyl Compounds into a Methylene Group by NH3BH3 or NaBH4 Catalyzed by Au Nanoparticles." Nanomaterials 11, no. 1 (January 18, 2021): 248. http://dx.doi.org/10.3390/nano11010248.

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Supported Au nanoparticles on TiO2 (1 mol%) are capable of catalyzing the reduction of the carbene-like diazo functionality of α-diazocarbonyl compounds into a methylene group [C=(N2) → CH2] by NH3BH3 or NaBH4 in methanol as solvent. The Au-catalyzed reduction that occurs within a few minutes at room temperature formally requires one hydride equivalent (B-H) and one proton that originates from the protic solvent. This pathway is in contrast to the Pt/CeO2-catalyzed reaction of α-diazocarbonyl compounds with NH3BH3 in methanol, which leads to the corresponding hydrazones instead. Under our stoichiometric Au-catalyzed reaction conditions, the ketone-type carbonyls remain intact, which is in contrast to the uncatalyzed conditions where they are selectively reduced by the boron hydride reagent. It is proposed that the transformation occurs via the formation of chemisorbed carbenes on Au nanoparticles, having proximally activated the boron hydride reagent. This protocol is the first general example of catalytic transfer hydrogenation of the carbene-like α -ketodiazo functionality.

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17

Wang, Jie, Wang-Bin Sun, Ying-Zi Li, Xuan Wang, Bing-Feng Sun, Guo-Qiang Lin, and Jian-Ping Zou. "A concise formal synthesis of platencin." Organic Chemistry Frontiers 2, no. 6 (2015): 674–76. http://dx.doi.org/10.1039/c5qo00065c.

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18

Yu, Jin-Sheng, and Jian Zhou. "A highly efficient Mukaiyama–Mannich reaction of N-Boc isatin ketimines and other active cyclic ketimines using difluoroenol silyl ethers catalyzed by Ph3PAuOTf." Organic & Biomolecular Chemistry 13, no. 45 (2015): 10968–72. http://dx.doi.org/10.1039/c5ob01895a.

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19

Qian, Deyun, and Junliang Zhang. "Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions." Beilstein Journal of Organic Chemistry 7 (June 15, 2011): 808–12. http://dx.doi.org/10.3762/bjoc.7.92.

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A straightforward, efficient, and reliable redox catalyst system for the Au(I)/Au(III)-catalyzed Sonogashira cross-coupling reaction of functionalized terminal alkynes with arylboronic acids under mild conditions has been developed.

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20

Li, Pan, Bingbing Ma, Liangbao Yang, and Jinhuai Liu. "Hybrid single nanoreactor for in situ SERS monitoring of plasmon-driven and small Au nanoparticles catalyzed reactions." Chemical Communications 51, no. 57 (2015): 11394–97. http://dx.doi.org/10.1039/c5cc03792a.

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21

Brand, Jonathan P., Clara Chevalley, and Jérôme Waser. "One-pot gold-catalyzed synthesis of 3-silylethynyl indoles from unprotected o-alkynylanilines." Beilstein Journal of Organic Chemistry 7 (May 4, 2011): 565–69. http://dx.doi.org/10.3762/bjoc.7.65.

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The Au(III)-catalyzed cyclization of 2-alkynylanilines was combined in a one-pot procedure with the Au(I)-catalyzed C3-selective direct alkynylation of indoles using the benziodoxolone reagent TIPS-EBX to give a mild, easy and straightforward entry to 2-substituted-3-alkynylindoles. The reaction can be applied to unprotected anilines, was tolerant to functional groups and easy to carry out (RT, and requires neither an inert atmosphere nor special solvents).

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22

Barabé, Francis, Patrick Levesque, Boubacar Sow, Gabriel Bellavance, Geneviève Bétournay, and Louis Barriault. "Gold(I)-catalyzed formation of bridged and fused carbocycles." Pure and Applied Chemistry 85, no. 6 (May 10, 2013): 1161–73. http://dx.doi.org/10.1351/pac-con-13-01-02.

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For many years, despite a rich coordination chemistry, gold (Au) was judged as being catalytically inactive for the formation of carbon–carbon bonds. In mid-1970, few reports demonstrated that Au salts could be very useful reagents to catalyze organic transformations. In recent years, homogeneous catalysis by Au has received considerable attention by the scientific community. It was shown that Au(I) or (III) catalysts are specific and more reactive than most of the other soft Lewis acids such as Hg(II), Cu(II), Pt(II), and Pd(II). Taking advantage of the affinity of cationic phosphine Au complexes to triple bonds, we conceived a Au(I)-catalyzed 6-endo-dig cyclization of cyclic enol ether to prepare bridged and fused bicyclic ketone. Keeping in mind that 5-exo-dig cyclizations can be a competitive process, we surveyed various Au(I) complexes.

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23

Ding, Liangbing, Feng Xiong, Yuekang Jin, Zhengming Wang, Guanghui Sun, and Weixin Huang. "Surface reaction network of CO oxidation on CeO2/Au(110) inverse model catalysts." Physical Chemistry Chemical Physics 18, no. 47 (2016): 32551–59. http://dx.doi.org/10.1039/c6cp05951a.

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24

Taskaya, Sultan, Nurettin Menges, and Metin Balci. "Gold-catalyzed formation of pyrrolo- and indolo-oxazin-1-one derivatives: The key structure of some marine natural products." Beilstein Journal of Organic Chemistry 11 (May 28, 2015): 897–905. http://dx.doi.org/10.3762/bjoc.11.101.

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Various N-propargylpyrrole and indolecarboxylic acids were efficiently converted into 3,4-dihydropyrrolo- and indolo-oxazin-1-one derivatives by a gold(III)-catalyzed cyclization reaction. Some of the products underwent TFA-catalyzed double bond isomerization and some did not. Cyclization reactions in the presence of alcohol catalyzed by Au(I) resulted in the formation of hemiacetals after cascade reactions.

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25

Fructos, Manuel R., Juan Urbano, M. Mar Díaz-Requejo, and Pedro J. Pérez. "Evidencing an inner-sphere mechanism for NHC-Au(I)-catalyzed carbene-transfer reactions from ethyl diazoacetate." Beilstein Journal of Organic Chemistry 11 (November 20, 2015): 2254–60. http://dx.doi.org/10.3762/bjoc.11.245.

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Kinetic experiments based on the measurement of nitrogen evolution in the reaction of ethyl diazoacetate (N2CHCO2Et, EDA) and styrene or methanol catalyzed by the [IPrAu]+ core (IPr = 1,3-bis(diisopropylphenyl)imidazole-2-ylidene) have provided evidence that the transfer of the carbene group CHCO2Et to the substrate (styrene or methanol) takes place in the coordination sphere of Au(I) by means of an inner-sphere mechanism, in contrast to the generally accepted proposal of outer-sphere mechanisms for Au(I)-catalyzed reactions.

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26

Tong, Zixuan, Olivia L. Garry, Philip J. Smith, Yubo Jiang, Steven J. Mansfield, and Edward A. Anderson. "Au(I)-Catalyzed Oxidative Functionalization of Yndiamides." Organic Letters 23, no. 12 (June 3, 2021): 4888–92. http://dx.doi.org/10.1021/acs.orglett.1c01625.

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27

Algasinger, Michael, Maximilian Bernt, Svetoslav Koynov, and Martin Stutzmann. "Porous silicon formation during Au-catalyzed etching." Journal of Applied Physics 115, no. 16 (April 28, 2014): 164308. http://dx.doi.org/10.1063/1.4873892.

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28

Wu, Jinsong, Sonal Padalkar, Sujing Xie, Eric R. Hemesath, Jipeng Cheng, George Liu, Aiming Yan, et al. "Electron Tomography of Au-Catalyzed Semiconductor Nanowires." Journal of Physical Chemistry C 117, no. 2 (January 4, 2013): 1059–63. http://dx.doi.org/10.1021/jp310816f.

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29

Kung, Mayfair C., Robert J. Davis, and Harold H. Kung. "Understanding Au-Catalyzed Low-Temperature CO Oxidation." Journal of Physical Chemistry C 111, no. 32 (July 11, 2007): 11767–75. http://dx.doi.org/10.1021/jp072102i.

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30

Genêt, J. P., V. Michelet, P. Toullec, E. Genin, and L. Leseurre. "Au(I)-Catalyzed Diastereoselective Tandem Addition/Carbocyclization." Synfacts 2007, no. 1 (January 2007): 0048. http://dx.doi.org/10.1055/s-2006-955730.

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31

Dembinski, R., Y. Li, and K. Wheeler. "Au/Ag-Catalyzed Synthesis of 3-Fluorofurans." Synfacts 2011, no. 02 (January 19, 2011): 0131. http://dx.doi.org/10.1055/s-0030-1259375.

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32

Chan, S. K., Y. Cai, I. K. Sou, and N. Wang. "MBE-grown Au-island-catalyzed ZnSe nanowires." Journal of Crystal Growth 278, no. 1-4 (May 2005): 146–50. http://dx.doi.org/10.1016/j.jcrysgro.2004.12.108.

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33

Goodwin, Justin A., and Aaron Aponick. "Regioselectivity in the Au-catalyzed hydration and hydroalkoxylation of alkynes." Chemical Communications 51, no. 42 (2015): 8730–41. http://dx.doi.org/10.1039/c5cc00120j.

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34

Wu, Qingshi, Han Cheng, Aiping Chang, Wenting Xu, Fan Lu, and Weitai Wu. "Glucose-mediated catalysis of Au nanoparticles in microgels." Chemical Communications 51, no. 89 (2015): 16068–71. http://dx.doi.org/10.1039/c5cc06386h.

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35

OVERBURY, S., V. SCHWARTZ, D. MULLINS, W. YAN, and S. DAI. "Evaluation of the Au size effect: CO oxidation catalyzed by Au/TiO2." Journal of Catalysis 241, no. 1 (July 1, 2006): 56–65. http://dx.doi.org/10.1016/j.jcat.2006.04.018.

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36

Kim, C. C., J. K. Kim, J. L. Lee, J. H. Je, M. S. Yi, D. Y. Noh, Y. Hwu, and P. Ruterana. "Au Catalyzed Structural and Electrical Evolution of Ni/Au Contact to GaN." physica status solidi (a) 188, no. 1 (November 2001): 379–82. http://dx.doi.org/10.1002/1521-396x(200111)188:1<379::aid-pssa379>3.0.co;2-u.

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37

Sheppard, Tom D. "Complexity-generating hydration reactions via gold-catalyzed addition of boronic acids to alkynes." Pure and Applied Chemistry 84, no. 11 (June 24, 2012): 2431–41. http://dx.doi.org/10.1351/pac-con-12-01-08.

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Boronic acids can serve as organic soluble substitutes for water molecules in the metal-catalyzed hydration of alkynes. The Au-catalyzed addition of boronic acids to alkynes provides an alternative method for enolate generation, which proceeds under exceptionally mild conditions. The resulting enolates can be trapped by aldehydes present in the reaction mixture, giving aldol products that can be isolated as cyclic borate esters. These compounds are versatile synthetic intermediates that can be elaborated into a variety of products by transformation of the boron moiety. The Au-catalyzed reaction of boronic acids with propargylic alcohols results in efficient Meyer–Schuster rearrangement to the corresponding enones. The rearrangement of tertiary alcohols gives (E)-enones with moderate to good selectivity, and the addition of a boronic acid to the reaction appears to enhance the level of geometrical control. The rearrangement of primary alcohols to terminal enones also occurs readily in the presence of catalytic Au(I) and a boronic acid, and the resulting terminal enones can be reacted with nucleophiles in one-pot procedures to give a variety of β-substituted ketones.

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38

Goodwin, Justin A., and Aaron Aponick. "Correction: Regioselectivity in the Au-catalyzed hydration and hydroalkoxylation of alkynes." Chemical Communications 52, no. 40 (2016): 6731. http://dx.doi.org/10.1039/c6cc90121b.

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39

Luo, Cuicui, Hongwei Yang, Rongfang Mao, Chunxu Lu, and Guangbin Cheng. "An efficient Au(i) catalyst for double hydroarylation of alkynes with heteroarenes." New Journal of Chemistry 39, no. 5 (2015): 3417–23. http://dx.doi.org/10.1039/c4nj02170c.

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40

Cai, Rong, Dawei Wang, Yunfeng Chen, Wuming Yan, Natalie R. Geise, Sripadh Sharma, Huiyuan Li, Jeffrey L. Petersen, Minyong Li, and Xiaodong Shi. "Facile synthesis of fluorescent active triazapentalenes through gold-catalyzed triazole–alkyne cyclization." Chem. Commun. 50, no. 55 (2014): 7303–5. http://dx.doi.org/10.1039/c4cc03175j.

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41

Nguyen, Duy Trinh, Nguyen Phu Thuong Nhan, Tran Thien Hien, Nguyen Dai Hai, Dai Viet N. Vo, and Long Giang Bach. "A Simple Approach for Immobilization of Fe-Core/Au-Shell Magnetic Nanoparticles on Multi-Walled Carbon Nanotubes via Cu(I) Huisgen Cycloaddition: Preparation and Characterization." Solid State Phenomena 279 (August 2018): 187–91. http://dx.doi.org/10.4028/www.scientific.net/ssp.279.187.

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In this report, we demonstrated a novel efficient a simple strategy route for the preparation of smart hybrid Fe-core/Au-shell magnetic onto multi-walled carbon nanotubes (CNT) sidewalls via Cu (I)-catalyzed 1, 3-dipolar cycloaddition (“click” coupling). The fabrication of gold-coated iron nanoparticles (Fe@AuNPs) is initially achieved by employing a two-step reverse micelle process. A new azide terminated ligand was first synthesized to change Fe@AuNPs by ligand exchange reaction. The Fe@Au NPs decorated MWNTs (MWNTs-Fe@Au) nanohybrids were synthesized by the reaction of an azide-containing Fe@Au NPs with alkyne-functionalized MWNTs via the Cu (I)-catalyzed 1,3-dipolar cycloaddition reaction. Energy dispersive X-ray (EDX) spectroscopy, Fourier transform infrared spectroscopy (FT-IR), and Transmission electron microscopy (HR-TEM) were used to study the changes in surface functionalities and demonstrate the successful immobilization of Fe@Au on CNT surface. In addition, the superconducting quantum interference device (SQUID) study revealed that the nanohybrids possess superparamagnetic character which is susceptible to rapid separation under an external magnetic field.

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42

Zhu, Dapeng, Xin Cao, and Biao Yu. "Au(i) π-bis(tert-butyldimethylsilyl)acetylene triphenylphosphine complex, an effective pre-catalyst for Au(i)-catalyzed reactions." Organic Chemistry Frontiers 2, no. 4 (2015): 360–65. http://dx.doi.org/10.1039/c5qo00023h.

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43

Liu, Congrong, Jin Xu, Lianghui Ding, Haiyun Zhang, Yunbo Xue, and Fulai Yang. "Au-Catalyzed tandem intermolecular hydroalkoxylation/Claisen rearrangement between allylic alcohols and chloroalkynes." Organic & Biomolecular Chemistry 17, no. 18 (2019): 4435–39. http://dx.doi.org/10.1039/c9ob00151d.

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44

Lau, Vivian M., Craig F. Gorin, and Matthew W. Kanan. "Electrostatic control of regioselectivity via ion pairing in a Au(i)-catalyzed rearrangement." Chem. Sci. 5, no. 12 (2014): 4975–79. http://dx.doi.org/10.1039/c4sc02058h.

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45

Liu, Yongxiang, Jia Guo, Yang Liu, Xiaoyu Wang, Yanshi Wang, Xinyu Jia, Gaofei Wei, Lizhu Chen, Jianyong Xiao, and Maosheng Cheng. "Au(i)-catalyzed triple bond alkoxylation/dienolether aromaticity-driven cascade cyclization to naphthalenes." Chem. Commun. 50, no. 47 (2014): 6243–45. http://dx.doi.org/10.1039/c4cc00464g.

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46

Jeon, Min Ho, Bijoy P. Mathew, Malleswara Rao Kuram, Kyungjae Myung, and Sung You Hong. "A palladium and gold catalytic system enables direct access to O- and S-linked non-natural glyco-conjugates." Organic & Biomolecular Chemistry 14, no. 48 (2016): 11518–24. http://dx.doi.org/10.1039/c6ob02437h.

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47

Liu, Yanhong, Yiying Yang, Rongxiu Zhu, Chengbu Liu, and Dongju Zhang. "Computational study on the 1,3-diyne synthesis from gold(i)-catalyzed alkynylation of terminal alkynes with alkynyl hypervalent iodine reagents under the aid of a silver complex and 1,10-phenanthroline." Catalysis Science & Technology 9, no. 15 (2019): 4091–99. http://dx.doi.org/10.1039/c9cy01067j.

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48

Waheed, Ammara, Changhai Cao, Yifei Zhang, Kai Zheng, and Gao Li. "Insight into Au/ZnO catalyzed aerobic benzyl alcohol oxidation by modulation–excitation attenuated total reflection IR spectroscopy." New Journal of Chemistry 46, no. 11 (2022): 5361–67. http://dx.doi.org/10.1039/d2nj00176d.

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49

Ma, Can-Liang, Xiao-Hua Li, Xiao-Long Yu, Xiao-Long Zhu, Yong-Zhou Hu, Xiao-Wu Dong, Bin Tan, and Xin-Yuan Liu. "Gold-catalyzed tandem synthesis of bioactive spiro-dipyrroloquinolines and its application in the one-step synthesis of incargranine B aglycone and seneciobipyrrolidine (I)." Organic Chemistry Frontiers 3, no. 3 (2016): 324–29. http://dx.doi.org/10.1039/c5qo00354g.

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50

Xi, Yumeng, Qiaoyi Wang, Yijin Su, Minyong Li, and Xiaodong Shi. "Quantitative kinetic investigation of triazole–gold(i) complex catalyzed [3,3]-rearrangement of propargyl ester." Chem. Commun. 50, no. 17 (2014): 2158–60. http://dx.doi.org/10.1039/c3cc49351b.

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