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Collect. Czech. Chem. Commun. 2010, 75, 607-615
Published online 2010-05-24 11:51:00

Protection of hydroxy groups as trimethylsilyl ethers using 1,1,1,3,3,3-hexamethyldisilazane (HMDS) catalyzed by poly(4-vinylpyridinium tribromide)

Arash Ghorbani-Choghamarania,*, Mohammad Ali Zolfigolb, Maryam Hajjamib, Khorshid Darvishia and Laleh Gholamniaa

a Department of Chemistry, Faculty of Science, Ilam University, P.O. Box 69315516, Ilam, Iran
b Faculty of Chemistry, Bu-Ali Sina University, P.O. Box 6517838683, Hamadan, Iran

Crossref Cited-by Linking

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  • Yadegari Maryam, Moghadam Majid, Tangestaninejad Shahram, Mirkhani Valiollah, Mohammadpoor-Baltork Iraj: Highly efficient and chemoselective trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) catalyzed by reusable electron-deficient [TiIV(salophen)(OTf)2]. Polyedron 2012, 31, 332. <>
  • Jereb Marjan: Highly atom economical uncatalysed and I2-catalysed silylation of phenols, alcohols and carbohydrates, using HMDS under solvent-free reaction conditions (SFRC). Tetrahedron 2012, 68, 3861. <>
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  • Lee Sang‐Hyeup, Kadam Santosh T.: Cross‐linked poly(4‐vinylpyridine/styrene) copolymer‐supported bismuth(III) triflate: an efficient heterogeneous catalyst for silylation of alcohols and phenols with HMDS. Applied Organom Chemis 2011, 25, 608. <>
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  • Ghorbani‐Choghamarani Arash, Zolfigol Mohammad Ali, Hajjami Maryam, Darvishi Khorshid, Gholamnia Laleh: ChemInform Abstract: Protection of Hydroxy Groups as Trimethylsilyl Ethers Using 1,1,1,3,3,3‐Hexamethyldisilazane (HMDS) Catalyzed by Poly(4‐vinylpyridinium tribromide). ChemInform 2010, 41. <>