Статті в журналах з теми "Au-catalyzed"
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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.
Повний текст джерелаRodriguez, 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.
Повний текст джерелаReeves, 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.
Повний текст джерелаShi, 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.
Повний текст джерелаЛещенко, Е. Д., та В. Г. Дубровский. "Моделирование профиля состава осевой гетероструктуры InSb/GaInSb/InSb в нитевидных нанокристаллах". Письма в журнал технической физики 48, № 19 (2022): 20. http://dx.doi.org/10.21883/pjtf.2022.19.53590.19339.
Повний текст джерелаLeshchenko 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.
Повний текст джерелаBhunia, 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.
Повний текст джерелаDubrovskii, 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.
Повний текст джерелаXu, 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.
Повний текст джерелаAponick, 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.
Повний текст джерелаKanjanachuchai, 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.
Повний текст джерелаHo, 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.
Повний текст джерелаGarcía‐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.
Повний текст джерелаBhattacharjee, 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.
Повний текст джерелаKumar, 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.
Повний текст джерелаKidonakis, Marios, та 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, № 1 (18 січня 2021): 248. http://dx.doi.org/10.3390/nano11010248.
Повний текст джерелаWang, 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.
Повний текст джерелаYu, 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.
Повний текст джерелаQian, 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.
Повний текст джерелаLi, 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.
Повний текст джерелаBrand, 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.
Повний текст джерелаBarabé, 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.
Повний текст джерелаDing, 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.
Повний текст джерелаTaskaya, 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.
Повний текст джерелаFructos, 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.
Повний текст джерелаTong, 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.
Повний текст джерелаAlgasinger, 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.
Повний текст джерелаWu, 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.
Повний текст джерелаKung, 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.
Повний текст джерелаGenêt, 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.
Повний текст джерелаDembinski, 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.
Повний текст джерелаChan, 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.
Повний текст джерелаGoodwin, 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.
Повний текст джерелаWu, 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.
Повний текст джерелаOVERBURY, 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.
Повний текст джерелаKim, 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.
Повний текст джерелаSheppard, 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.
Повний текст джерелаGoodwin, 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.
Повний текст джерелаLuo, 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.
Повний текст джерелаCai, 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.
Повний текст джерелаNguyen, 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.
Повний текст джерелаZhu, Dapeng, Xin Cao та Biao Yu. "Au(i) π-bis(tert-butyldimethylsilyl)acetylene triphenylphosphine complex, an effective pre-catalyst for Au(i)-catalyzed reactions". Organic Chemistry Frontiers 2, № 4 (2015): 360–65. http://dx.doi.org/10.1039/c5qo00023h.
Повний текст джерелаLiu, 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.
Повний текст джерелаLau, 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.
Повний текст джерелаLiu, 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.
Повний текст джерелаJeon, 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.
Повний текст джерелаLiu, 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.
Повний текст джерелаWaheed, 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.
Повний текст джерелаMa, 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.
Повний текст джерелаXi, 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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