[1] I. Agirre, M.B. Güemez, A. Ugarte, J. Requies, V.L. Barrio, J.F. Cambra, P.L. Arias, Kinetics of acetalization of perfumery aldehydes with alkanols over solid acid catalysts, Fuel Process. Technol. 116 (2013) 182-188.[2] F. Frusteri, L. Spadaro, C. Beatrice, C. Guido, Oxygenated additives production for diesel engine emission improvement, Chem. Eng. J. 134 (2007) 239-245.[3] K. Stanis?aw, P. Mateusz, S. Krzysztof, K. Ewelina, Transition metal compounds and complexes as catalysts in synthesis of acetals and orthoesters: theoretical, mechanistic and practical aspects, Coord. Chem. Rev. 256 (2012) 2057-2095.[4] M.R. Capeletti, L. Balzano, G. de la Puente, M. Laborde, U. Sedran, Synthesis of acetal (1,1-diethoxyethane) from ethanol and acetaldehyde over acidic catalysts, Appl. Catal. A Gen. 198 (2000) 1-4.[5] B.Wang, Y. Gu, G. Song, T. Yang, L. Yang, J. Suo, Sulfamic acid as a cost-effective and recyclable catalyst for liquid Beckmann rearrangement, a green process to produce amides from ketoximes without waste, ChemInform 35 (2004).[6] Y.X. Cheng, Y.Y. Zhou, J.D. Zhang, X.D. Fei,M.A. Tengzhou, X.Z. Liang, Synthesis of a novel solid acidwith both sulfonic and carbonyl acid groups and its catalytic activities in acetalization, Chin. J. Chem. Eng. 22 (2014) 312-317.[7] Y.Wang, X. Gong, Z.Wang, L. Dai, SO3H-functionalized ionic liquids as efficient and recyclable catalysts for the synthesis of pentaerythritol diacetals and diketals, J. Mol. Catal. A Chem. 322 (2010) 7-16.[8] M.R. Capeletti, L. Balzano, G. de la Puente, M. Laborde, U. Sedran, Synthesis of acetal (1,1-diethoxyethane) from ethanol and acetaldehyde over acidic catalysts, Appl. Catal. A Gen. 198 (2000) L1-L4.[9] Z.J. Yang, H. Zeng, X.T. Zhou, H.B. Ji, Mechanism into selective oxidation of cinnamaldehyde using β-cyclodextrin polymer as phase-transfer catalyst, Tetrahedron 68 (2012) 5912-5919.[10] H.Y. Chen, H.B. Ji, β-Cyclodextrin promoted oxidation of cinnamaldehyde to natural benzaldehyde in water, Chin. J. Chem. Eng. 19 (2011) 972-977.[11] E. Schneiderman, A.M. Stalcup, Cyclodextrins: A versatile tool in separation science, J. Chromatogr. B 745 (2000) 83-102.[12] N. Srilakshmi Krishnaveni, K. Surendra, V. Pavan Kumar, β-Cyclodextrin promoted allylation of aldehydes with allyltributyltin under supramolecular catalysis in water, Tetrahedron Lett. 46 (2005) 4299-4301.[13] K. Surendra, N. Srilakshmi Krishnaveni, K. Rama Rao, Direct Barbier-type allylation of aromatic acetals and dioxolanes in the presence of β-cyclodextrin inwater, Tetrahedron Lett. 47 (2006) 2133-2136.[14] M. Somi Reddy, M. Narender, K. Rama Rao, A mild and efficient synthesis of α-tosylamino ketones from aryl aziridines in the presence of β-cyclodextrin and NBS in water, Tetrahedron Lett. 46 (2005) 1299-1301.[15] M. Narender,M. Somi Reddy, V. Pavan Kumar, Y.V.D. Nageswar, K. Rama Rao, Direct synthesis of carbonyl compounds from THP ethers with IBX in the presence of β-cyclodextrin in water, Tetrahedron Lett. 46 (2005) 1971-1973.[16] K. Surendra, N.S. Krishnaveni, V. Pavan Kumar, R. Sridhar, K. Rama Rao, Selective and efficient oxidation of sulfides to sulfoxides with N-bromosuccinimide in the presence of β-cyclodextrin in water, Tetrahedron Lett. 46 (2005) 4581-4583.[17] K. Surendra, N.S. Krishnaveni,M.A. Reddy, Y.V. Nageswar, K.R. Rao, Mild oxidation of alcohols with o-iodoxybenzoic acid (IBX) in water/acetone mixture in the presence of β-cyclodextrin, J. Org. Chem. 68 (2003) 2058-2059.[18] H.B. Ji, D.P. Shi, M. Shao, Z. Li, L.F. Wang, Transition metal-free and substrateselective oxidation of alcohols using water as an only solvent in the presence of β-cyclodextrin, Tetrahedron Lett. 46 (2005) 2517-2520.[19] M. Narender, M. Somi Reddy, R. Sridhar, Y.V.D. Nageswar, K. Rama Rao, Aqueous phase synthesis of thiazoles and aminothiazoles in the presence of β-cyclodextrin, Tetrahedron Lett. 46 (2005) 5953-5955.[20] H.Y. Chen, H.B. Ji, X.T. Zhou, L.F. Wang, Green synthesis of natural benzaldehyde from cinnamon oil catalyzed by hydroxypropyl-β-cyclodextrin, Tetrahedron 66 (2010) 9888-9893.[21] N. Srilakshmi Krishnaveni, K. Surendra, M. Arjun Reddy, Y.V.D. Nageswar, K. Rama Rao, Highly efficient deprotection of aromatic acetals under neutral conditions using β-cyclodextrin in water, J. Org. Chem. 68 (2003) 2018-2019.[22] H.G. Jiang, Z.J. Yang, X.T. Zhou, Y.X. Fang, H.B. Ji, Immobilization of β-cyclodextrin as insoluble β-cyclodextrin polymer and its catalytic performance, Chin. J. Chem. Eng. 20 (2012) 784-792. |