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- Quick photo-Fenton degradation of phenolic compounds by Cu/Al2O3–MCM-41 under visible light irradiation: small particle size, stabilization of copper, easy reducibility of Cu and visible light active material. Amaresh C. Pradhan, Binita Nanda, K. M. Parida, Mira Das
, Dalton Trans.
, 2013
, 42
, 558
- A review on the recent progress, challenges and perspective of layered double hydroxides as promising photocatalysts. Lagnamayee Mohapatra, Kulamani Parida
, J. Mater. Chem. A
, 2016
, 4
, 10744
- Three-state molecular shuttles operated using acid/base stimuli with distinct outputs. Yuji Tokunaga, Masanori Kawabata, Naoki Matsubara
, Org. Biomol. Chem.
, 2011
, 9
, 4948
- Degradation of roxarsone in a sulfate radical mediated oxidation process and formation of polynitrated by-products. Yuefei Ji, Yuanyuan Shi, Deyang Kong, Junhe Lu
, RSC Adv.
, 2016
, 6
, 82040
- Evaluating N-benzylgalactonoamidines as putative transition state analogs for β-galactoside hydrolysis. Qiu-Hua Fan, Susanne Striegler, Rebekah G. Langston, James D. Barnett
, Org. Biomol. Chem.
, 2014
, 12
, 2792
- Mechanism of formation of 4-methyl- and 4-chloro-2-nitrophenol in the nitration of 4-methyl- and 4-chloro-anisole, respectively, in aqueous sulphuric acid. Roy B. Moodie, Kenneth Schofield, Geoffrey D. Tobin
, J. Chem. Soc., Chem. Commun.
, 1978
, 180
- Electrophilic aromatic substitution. Part 28. The mechanism of nitration of some 4-substituted anisoles and phenols, and of rearrangement of the intermediate 4-nitro-4-substituted-cyclohexa-2,5-dienones. Colin Bloomfield, Ajay K. Manglik, Roy B. Moodie, Kenneth Schofield, Geoffrey D. Tobin
, J. Chem. Soc., Perkin Trans. 2
, 1983
, 75
- 512. Kinetics and mechanism of aromatic nitration. Part VI. The nitration of phenols and phenolic ethers: the concomitant dealkylation of phenolic ethers. The role of nitrous acid. C. A. Bunton, E. D. Hughes, C. K. Ingold, D. I. H. Jacobs, M. H. Jones, G. J. Minkoff, R. I. Reed
, J. Chem. Soc.
, 1950
, 2628
- Proximity effects in diaryl derivatives. Part VI. Base-catalysed rearrangement of 2-(hydroxyamino)aryl aryl sulphones to 2-hydroxy-2′-(arylsulphonyl)azoxybenzenes. M. F. Grundon, D. J. Maitland, W. L. Matier
, J. Chem. Soc. C
, 1971
, 654
- XXI.—The chlorination of iodophenols. Part III. The chlorination of o-iodophenol. Samuel Buchan, Hamilton McCombie
, J. Chem. Soc.
, 1931
, 137