6
S. H. JAVADI ET AL.
[29] Gopinath, R.; Patel, B. K. Tetrabutylammonium Tribromide
(TBATB)ꢂmeOH: An Efficient Chemoselective Reagent for the
Cleavage of Tert-bButyldimethylsilyl (TBDMS) Ethers. Org.
[30] Karimi, B.; Zareyee, D. A High Loading Sulfonic Acid-function-
alized Ordered Nanoporous Silica as an Efficient and Recyclable
Catalyst for Chemoselective Deprotection of Tert-butyldime-
thylsilyl Ethers. Tetrahedron Lett. 2005, 46, 4661–4665. DOI:
[31] Karimi, B.; Zamani, A.; Zareyee, D. N-Iodosuccinimide (NIS) as
a Mild and Highly Chemoselective Catalyst for Deprotection of
Tert-butyldimethylsilyl Ethers. Tetrahedron Lett. 2004, 45,
[32] Shah, S. T. A.; Singh, S.; Guiry, P. J. A Novel, chemoselective
and Efficient Microwave-assisted Deprotection of Silyl Ethers
with Selectfluor. J. Org. Chem. 2009, 74, 2179–2182. DOI:
Amorphous Carbon Bearing SO3H, COOH, and OH Groups. J.
Am. Chem. Soc. 2009, 131, 12787–12793. DOI: 10.1021/
[48] Zareyee, D.; Moosavi, S. M.; Alaminezhad, A. Chemoselective
Synthesis of Geminal Diacetates (acylals) using Eco-friendly
Reusable Propylsulfonic Acid Based Nanosilica (SBA-15-Ph-
PrSO3H) under Solvent-Free. J. Mol. Catal. A: Chem. 2013, 378,
[49] Margolese, D.; Melero, J. A.; Christiansen, S. C.; Chmelka, B. F.;
Stucky, G. D. Direct Syntheses of Ordered SBA-15 Mesoporous
Silica Containing Sulfonic Acid Groups. Chem. Mater. 2000, 12,
[50] Karimi, B.; Zareyee, D. Solvent-free Three Component Strecker
Reaction of Ketones Using Highly Recyclable and Hydrophobic
Sulfonic Acid Based Nanoreactors. J. Mater. Chem. 2009, 19,
[51] Karimi, B.; Zareyee, D. Design of a Highly Efficient and Water-
tolerant Sulfonic Acid Nanoreactor Based on Tunable Ordered
Porous Silica for the Von Pechmann Reaction. Org. Lett. 2008,
[33] Bhure, M. H.; Kumar, I.; Natu, A. D.; Rode, C. V. Facile and
Highly Selective Deprotection of Tert-butyldimethylsilyl Ethers
Using Sulfated SnO2 as a Solid Catalyst. Synth. Commun. 2008,
[52] Gu, Y.; Karam, A.; Jerome, F.; Barrault, J. Selectivity
Enhancement of Silica-supported Sulfonic Acid Catalysts in
Water by Coating of Ionic Liquid. Org. Lett. 2007, 9,
[34] Olah, G. A.; Pradeep, S. I.; Prakash, G. K. S. Perfluorinated
R
V
Resinsulfonic Acid (nafion-H ) Catalysis in Synthesis. Synthesis
[35] Corma, A. Inorganic Solid Acids and Their Use in Acid-cata- [53] Sch€atz, A.; Reiser, O.; Stark, W. J. Nanoparticles as Semi-het-
lyzed Hydrocarbon Reactions. Chem. Rev. 1995, 95, 559–614.
erogeneous Catalyst Supports. Chem. Eur. J. 2010, 16,
[36] Herron, N.; Farneth, W. E. The Design and Synthesis of [54] Lee, J.; Lee, Y.; Youn, J. K.; Na, H. B.; Yu, T.; Kim, H.; Lee,
Heterogeneous Catalyst Systems. Adv. Mater. 1996, 8, 959–968.
[37] Horsley, J. A. Producing Bulk and Fine Chemicals Using Solid
Acids. CHEMTECH 1997, 27, 45–49.
[38] Corma, A.; Garcia, H. Organic Reactions Catalyzed over Solid
[39] Tanabe, K.; Holderich, W. F. Industrial Application of Solid
Acid–base Catalysts. Appl. Catal. A. 1999, 181, 399–434. DOI:
S. M.; Koo, Y. M.; Kwak, J. H.; Park, H. G.; et al. Simple
Synthesis of Functionalized Superparamagnetic Magnetite/silica
Core/shell Nanoparticles and Their Application as Magnetically
Separable High-performance Biocatalysts. Small 2008, 4,
143–152. DOI: 0.1002/smll.200700456. DOI: 10.1002/
[55] Lu, A.; Salabas, E. L.; Schuth, F. Magnetic Nanoparticles: syn-
thesis, protection, functionalization, and Application. Angew.
Chem. Int. Ed. 2007, 46, 1222–1224. DOI: 10.1002/
[40] Sheldon, R. A.; Van Bekkum, H. Fine Chemicals through [56] Wang, D.; Astruc, D. Fast-growing Field of Magnetically
Heterogeneous Catalysis. Wiley-VCH, Weinheim, 2001.
Recyclable Nanocatalysts. Chem. Rev. 2014, 114, 6949–3985.
[41] Li, Q.; Meng, F.; Zhang, B.; Tian, M.; Lian, J. Mesomorphic
Phases of Main-chain Liquid-crystalline Polymers with Pendent [57] Karimi, B.; Mansouri, F.; Mirzaei, H. M. Recent Applications of
Sulfonic Acid Groups. J. Appl. Polym. Sci. 2008, 110, 791–797.
[42] Caetano, C. S.; Guerreiro, L.; Fonseca, I. M.; Ramos, A. M.;
Magnetically Recoverable Nanocatalysts in C-C and C-X
Coupling Reactions. ChemCatChem. 2015, 7, 1736–1789. DOI:
Vital, J.; Castanheiro, J. E. Esterification of Fatty Acids to [58] Khazaei, A.; Sarmasti, N.; Yousefi Seyf, J. Anchoring High
Biodiesel over Polymers with Sulfonic Acid Groups. Appl.
Catal. A: Gen. 2009, 359, 41–46. DOI: 10.1016/
Density Sulfonic Acid Based Ionic Liquid on the Magnetic
Nano-magnetite (Fe3O4), Application to the Synthesis of
Hexahydroquinoline Derivatives. J. Mol. Liq. 2018, 262,
[43] Fukuhara, K.; Nakajima, K.; Kitano, M.; Kato, H.; Hayashi, S.;
Hara, M. Structure and Catalysis of Cellulose-Derived [59] Nemati, F.; Heravi, M. M.; Saeedi Rad, R. Nano-Fe3O4
Amorphous Carbon Bearing SO3H Groups. ChemSusChem.
[44] Zareyee, D.; Serehneh, M. Recyclable CMK-5 Supported
Sulfonic Acid as an Environmentally Benign Catalyst for
Solvent-free One-pot Construction of Coumarin through
Encapsulated-silica Particles Bearing Sulfonic Acid Groups as a
Magnetically Separable Catalyst for Highly Efficient
Knoevenagel Condensation and Michael Addition Reactions of
Aromatic Aldehydes with 1,3-cyclic Diketones. Chin. J. Catal.
Pechmann Condensation. J. Mol. Catal. A: Chem. 2014, 391, [60] Kabiri Esfahani, F.; Zareyee, D.; Yousefi, R. Sulfonated Core-
shell Magnetic Nanoparticle (Fe3O4@SiO2@PrSO3H) as
Highly Active and Durable Protonic Acid Catalyst; synthesis of
Coumarin Derivatives through Pechmann Reaction.
a
[45] Toda, M.; Takagaki, A.; Okamura, M.; Kondo, J. N.; Hayashi,
S.; Domen, K.; Hara, M. Biodiesel Made with Sugar Catalyst.
ChemCatChem. 2014, 6, 3333–3337. DOI: 10.1002/
[46] Zareyee, D.; Ghandali, M. S.; Khalilzadeh, M. A. Sulfonated
Ordered Nanoporous Carbon (CMK-5-SO3H) as an Efficient [61] Kabiri Esfahani, F.; Zareyee, D.; Shokuhi Rad, A.; Taher, -.;
and Highly Recyclable Catalyst for the Silylation of Alcohols
and Phenols with Hexamethyldisilazane (HMDS). Catal. Lett.
Bahrami, S. Sulfonic Acid Supported on Magnetic Nanoparticle
as an Eco-friendly, durable and Robust Catalyst for the
Synthesis of b-Amino Carbonyl Compounds through Solvent
Free Mannich Reaction. Appl. Organometal. Chem. 2017, 31,
[47] Suganuma, S.; Nakajima, K.; Kitano, M.; Yamaguchi, D.; Kato,
H.; Hayashi, S.; Hara, M. Hydrolysis of Cellulose by