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Conversion of aldehydes into geminal diacetates
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(a) Sandberg, M.; Sydnes, L. K. The chemistry of acylals: Part II. Formation of nitriles by treatment of acylals with trimethylsilyl azide in the presence of Lewis acid. Tetrahedron Lett. 1998, 39, 6361-6364;
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Palladium-catalysed substitution reactions of geminal allylic diacetates
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3, an efficient catalyst for formation and deprotectection of geminal diacetates (acylals); chemoselective protection of aldehydes in presence of ketones
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3, an efficient catalyst for formation and deprotectection of geminal diacetates (acylals); chemoselective protection of aldehydes in presence of ketones. Synlett 1998, 849-850.
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Iodine as acetylation catalyst in the preparation of 1,1-diacetates from aldehydes
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Deka, N.; Kalita, D. J.; Borah, R.; Sarmah, J. C. Iodine as acetylation catalyst in the preparation of 1,1-diacetates from aldehydes. J. Org. Chem. 1997, 62, 1563-1564.
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Deka, N.1
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Mild and efficient conversion of aldehydes to 1,1-diacetates catalysed with N-bromosuccinimide (NBS)
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Karimi, B.; Seradj, H.; Ebrahimian, G. R. Mild and efficient conversion of aldehydes to 1,1-diacetates catalysed with N-bromosuccinimide (NBS). Synlett 2000, 623-624.
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Diacetates from aldehydes in the presence of zeolites
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Pereira, C.; Gigante, B.; Marcclo Curto, M. J.; Carreyre, H.; Perot, G.; Guisnet, M. Diacetates from aldehydes in the presence of zeolites. Synthesis 1995, 1077-1078.
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40) as an efficient heterogeneous inorganic catalyst for the chemoselective synthesis of geminal diacetates (acylals) under solvent-free conditions
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40) as an efficient heterogeneous inorganic catalyst for the chemoselective synthesis of geminal diacetates (acylals) under solvent-free conditions. Tetrahedron Lett. 2003, 44, 3951-3954.
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An efficient method for the chemoselective synthesis of acylals from aromatic aldehydes using bismuth triflate
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Carrigan, M. D.; Eash, K. J.; Oswald, M. C.; Mohan, R. S. An efficient method for the chemoselective synthesis of acylals from aromatic aldehydes using bismuth triflate. Tetrahedron Lett. 2001, 42, 8133-8135.
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Solvent free organic synthesis
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Lithium chloride catalysed acetylation of alcohols, thiols, phenols and amines
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(a) Sabitha, G.; Reddy, B. V. S.; Srividya, R.; Yadav, R. S. Lithium chloride catalysed acetylation of alcohols, thiols, phenols and amines. Synth. Commun. 1999, 29, 2311-2315;
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Synthesis of allylic halides and 1,5-dienes from allylic alcohols
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(b) Stork, G.; Grieco, P. A.; Gregson, M. Synthesis of allylic halides and 1,5-dienes from allylic alcohols. Tetrahedron Lett. 1969, 1393-1395;
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Dehydrobromination of 1,2-dibromo-cyclohexane and related compounds by lithium carbonate in hexamethylphosphorictriamide. An improved synthesis of 1,3-cyclohexadiene and some deuterium labeled analogs
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(c) Weisz, A.; Mandelbaum, A. Dehydrobromination of 1,2-dibromo- cyclohexane and related compounds by lithium carbonate in hexamethylphosphorictriamide. An improved synthesis of 1,3-cyclohexadiene and some deuterium labeled analogs. J. Org. Chem. 1984, 49, 2648-2650;
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A mild and efficient method for selective deprotection of tetrahydropyranyl ethers to alcohols
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A highly regioselective conversion of epoxides to halohydrins by lithium halides
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4 catalysed conversion of aldehydes to geminal diacetates and dipivolates and their cleavage
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4 catalysed conversion of aldehydes to geminal diacetates and dipivolates and their cleavage. Tetrahedron 2003, 59, 9171-9576.
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An efficient and practical procedure for synthesis of 1,1-diacetates from aldehydes catalysed by zirconium sulphate tetrahydrate-silica gel
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Jin, T.; Feng, G.; Yang, M.; Li, T. An efficient and practical procedure for synthesis of 1,1-diacetates from aldehydes catalysed by zirconium sulphate tetrahydrate-silica gel. Synth. Commun. 2004, 34, 1645-1651.
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Metal cation exchanged montmorillonite catalysed protection of aromatic aldehydes with acetic anhydride
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Zinc-metal promoted selective α-haloacylation and gem-bisacylation of alkyl aldehydes in the presence of chlorotrimethylsilane
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Ishino, Y.; Mihara, M.; Takeuchi, T.; Takemoto, M. Zinc-metal promoted selective α-haloacylation and gem-bisacylation of alkyl aldehydes in the presence of chlorotrimethylsilane. Tetrahedron Lett. 2004, 45, 3503-3506.
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