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For: Tong J, Wang W, Su L, Li Q, Liu F, Ma W, Lei Z, Bo L. Highly selective oxidation of cyclohexene to 2-cyclohexene-1-one over polyoxometalate/metal–organic framework hybrids with greatly improved performances. Catal Sci Technol 2017;7:222-30. [DOI: 10.1039/c6cy01554a] [Cited by in Crossref: 36] [Cited by in F6Publishing: 37] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Heravi MM, Mirzaei M. Polyoxometalate-based host–guest framework materials. Polyoxometalate-Based Hybrids and their Applications 2023. [DOI: 10.1016/b978-0-323-91731-5.00004-4] [Reference Citation Analysis]
2 Uysal Karatas B. New reusable heterogeneous catalyst in the MPV reduction in cyclohexenones: moderate one-pot synthesis of cyclohexenols (effect of methyl substituents). J IRAN CHEM SOC 2022. [DOI: 10.1007/s13738-022-02698-2] [Reference Citation Analysis]
3 Heravi MM, Bamoharram FF. Supported heteropoly acids. Heteropolyacids as Highly Efficient and Green Catalysts Applied in Organic Transformations 2022. [DOI: 10.1016/b978-0-323-88441-9.00007-7] [Reference Citation Analysis]
4 Zhang Y, Liu Z, Guo C, Guo C, Lu Y, Wang J. Selective photocatalytic oxidation of cyclohexene coupled with hydrogen evolution from water splitting over Ni/NiO/CdS and mechanism insight. Catal Sci Technol . [DOI: 10.1039/d2cy00674j] [Reference Citation Analysis]
5 Wu Y, Su M, Xiao Y, Guang B, Liu Y. Heteropolyacid-Based Poly(ionic liquid)s for the Selective Oxidation of Cyclohexene to 2-Cyclohexene-1-one. Ind Eng Chem Res 2022;61:299-306. [DOI: 10.1021/acs.iecr.1c04108] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
6 Tang Z, Yu Y, Chen Z, Liu D, Fang N, Wu H, Liu Y, He M. Expanded titanosilicate MWW-related materials synthesized from a boron-containing precursor as an efficient catalyst for cyclohexene oxidation. Microporous and Mesoporous Materials 2021;327:111437. [DOI: 10.1016/j.micromeso.2021.111437] [Reference Citation Analysis]
7 Li HL, Lian C, Yang GY. A {Ti6W4}-Cluster-Substituted Polyoxotungstate: Synthesis, Structure, and Catalytic Oxidation Properties. Inorg Chem 2021;60:14622-8. [PMID: 34533302 DOI: 10.1021/acs.inorgchem.1c01643] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
8 Ghubayra R, Hindle R, Yahya R, Kozhevnikova EF, Kozhevnikov IV. Aerobic Oxidative Desulfurization of Liquid Fuel Catalyzed by P–Mo–V Heteropoly Acids in the Presence of Aldehyde. Catalysts 2021;11:988. [DOI: 10.3390/catal11080988] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
9 Rao BG, Sudarsanam P, Rao TV, Amin MH, Bhargava SK, Reddy BM. Highly Dispersed MnOx Nanoparticles on Shape-Controlled SiO2 Spheres for Ecofriendly Selective Allylic Oxidation of Cyclohexene. Catal Lett 2020;150:3023-35. [DOI: 10.1007/s10562-020-03205-z] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
10 Li H, Lian C, Chen L, Zhao J, Yang GY. Two unusual nanosized Nd3+-substituted selenotungstate aggregates simultaneously comprising lacunary Keggin and Dawson polyoxotungstate segments. Nanoscale 2020;12:16091-101. [PMID: 32724947 DOI: 10.1039/d0nr04051g] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 4.7] [Reference Citation Analysis]
11 Guo Y, Li P, Zou W, Zhang Y, Pan Y, Ruan R, Xiao L, Hou L. Remarkable binuclear Schiff‐based complex catalyze the epoxidation of alkenes: effects of substituent group. Appl Organomet Chem 2020;34. [DOI: 10.1002/aoc.5608] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
12 Jin M, Niu Q, Liu G, Lv Z, Si C, Guo H. Encapsulation of ionic liquids into POMs-based metal–organic frameworks: screening of POMs-ILs@MOF catalysts for efficient cycloolefins epoxidation. J Mater Sci 2020;55:8199-210. [DOI: 10.1007/s10853-020-04611-9] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 3.7] [Reference Citation Analysis]
13 Khanmohammadi Khorrami MR, Shokri Aghbolagh Z. Synthesis and non‐parametric evaluation studies on high performance of catalytic oxidation‐extraction desulfurization of gasoline using the novel TBAPW 11 Zn@TiO 2 @PAni nanocomposite. Appl Organometal Chem 2019;34. [DOI: 10.1002/aoc.5299] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
14 Shi X, Shi Z, Niu G, Si C, Han Q, Zhang J. A Bimetallic Pure Inorganic Framework for Highly Efficient and Selective Photocatalytic Oxidation of Cyclohexene to 2-Cyclohexen-1-ol. Catal Lett 2019;149:3048-57. [DOI: 10.1007/s10562-019-02847-y] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
15 Samaniyan M, Mirzaei M, Khajavian R, Eshtiagh-hosseini H, Streb C. Heterogeneous Catalysis by Polyoxometalates in Metal–Organic Frameworks. ACS Catal 2019;9:10174-91. [DOI: 10.1021/acscatal.9b03439] [Cited by in Crossref: 147] [Cited by in F6Publishing: 152] [Article Influence: 36.8] [Reference Citation Analysis]
16 Chen S, Xiang Y, Katherine Banks M, Xu W, Peng C, Wu R. Polyoxometalate-coupled graphene nanohybrid via gemini surfactants and its electrocatalytic property for nitrite. Applied Surface Science 2019;466:110-8. [DOI: 10.1016/j.apsusc.2018.09.246] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 4.5] [Reference Citation Analysis]
17 Aman R, Clearfield A, Sadiq M, Ali Z. HKUST-1 Supported on Zirconium Phosphate as an Efficient Catalyst for Solvent Free Oxidation of Cyclohexene: DFT Study. Catalysts 2018;8:546. [DOI: 10.3390/catal8110546] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
18 Kohantorabi M, Gholami MR. Cyclohexene oxidation catalyzed by flower-like core-shell Fe 3 O 4 @Au/metal organic frameworks nanocomposite. Materials Chemistry and Physics 2018;213:472-81. [DOI: 10.1016/j.matchemphys.2018.04.051] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 3.0] [Reference Citation Analysis]
19 Rao BG, Sudarsanam P, Nallappareddy PRG, Yugandhar Reddy M, Venkateshwar Rao T, Reddy BM. Selective allylic oxidation of cyclohexene over a novel nanostructured CeO2–Sm2O3/SiO2 catalyst. Res Chem Intermed 2018;44:6151-68. [DOI: 10.1007/s11164-018-3482-1] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.2] [Reference Citation Analysis]
20 Singh VK, Maurya A, Kesharwani N, Kachhap P, Kumari S, Mahato AK, Mishra VK, Haldar C. Synthesis, characterization, and catalytic oxidation of styrene, cyclohexene, allylbenzene, and cis -cyclooctene by recyclable polymer-grafted Schiff base complexes of vanadium(IV). Journal of Coordination Chemistry 2018;71:520-41. [DOI: 10.1080/00958972.2018.1434516] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
21 Govinda Rao B, Sudarsanam P, Nallappareddy P, Yugandhar Reddy M, Venkateshwar Rao T, Reddy BM. Selective allylic oxidation of cyclohexene catalyzed by nanostructured Ce-Sm-Si materials. Catalysis Communications 2017;101:57-61. [DOI: 10.1016/j.catcom.2017.07.027] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 2.0] [Reference Citation Analysis]
22 Ha PT, Le BT, To TC, Doan SH, Nguyen TT, Phan NT. Synthesis of aryl-substituted pyridines via cyclization of N,N-dialkylanilines with ketoxime carboxylates under metal-organic framework catalysis. Journal of Industrial and Engineering Chemistry 2017;54:151-61. [DOI: 10.1016/j.jiec.2017.05.028] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
23 Song Y, Xin F, Zhang L, Wang Y. Oxidation of Cyclohexene in the Presence of Transition-Metal-Substituted Phosphotungstates and Hydrogen Peroxide: Catalysis and Reaction Pathways. ChemCatChem 2017;9:4139-47. [DOI: 10.1002/cctc.201700856] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 2.8] [Reference Citation Analysis]