References
- Greene, T. W.; Wuts, P. G. Protective Group s in OrganicSynthesis, 3rd ed.; John Wiley & Sons Inc.: New York, 1991.
- Haslam, E. Tetrahedron 1980, 36, 2409. https://doi.org/10.1016/0040-4020(80)80219-5
- Muzler, J. Comprehensive Organic Synthesis; Trost, B. M.,Fleming, I., Eds.: Oxford: Pergamon Press: 1991; Vol. 6, p 323.
- Trost, B. M. Angew. Chem. Int. Ed. Engl. 1995, 34, 259. https://doi.org/10.1002/anie.199502591
- Izumi, J.; Shiina, I.; Mukaiyama, T. Chem. Lett. 1995, 141.
- Vedejs, E.; Daugulis, J. J. Org. Chem. 1996, 61, 5702. https://doi.org/10.1021/jo9609485
- Iranpoor, N.; Firouzabadi, H.; Zolfigol, M. A. Synth. Commun.1998, 28, 1923. https://doi.org/10.1080/00397919808007166
- Chandrasekahar, S.; Ramachander, T.; Takhi, M. Tetrahedron Lett.1998, 39, 3263. https://doi.org/10.1016/S0040-4039(98)00465-1
- Ganesam, B.; Small, V. R., Jr. J. Org. Chem. 1974, 39, 3728. https://doi.org/10.1021/jo00939a026
- Tyryshkin, N. I.; Vedernikov, A. N.; Solomonov, B. N.;Garifzyanova, G. G. J. Gen. Chem. USSR 1992, 62, 303.
- Ishihara, K.; Kubota, M.; Kurihara, H.; Yamamoto, H. J. Org.Chem. 1996, 61, 4560. https://doi.org/10.1021/jo952237x
- Ishihara, K.; Kubota, M.; Kurihara, H.; Yamamoto, H. Synlett1996, 265.
- Barrett, A. G. M.; Broddock, C. D. J. Chem. Soc., Chem.Commun. 1997, 351.
- Ringold, H. J.; Loeken, B.; Rosenkranz, G.; Sondheimer, F. J. Am. Chem. Soc. 1956, 76, 816.
- McOmie, J. F. W. Protective Groups in Organic Chemistry;Plenum: London, 1973; p 111.
- Caputo, R.; Ferreri, C.; Palumbo, G. Synth. Commun. 1987, 17,1629. https://doi.org/10.1080/00397918708057794
- Barluenga, J.; Campos, P. J.; Gonzalez-Nunez, E.; Asensio, G.Synthesis 1985, 425.
- Fernandez, I.; garica, B.; Munoz, S.; Pedro, J. R.; Salud, R. Synlett1993, 489.
- Katritzky, A. R.; Chang, H.-X.; Yang, B. Synthesis 1995, 503.
- Gramani, J. C.; Remuson, R. Synthesis 1982, 264.
- Neveux, M.; Bruneau, C.; Dixneuf, P. H. J. Chem. Soc., PerkinTrans. 1 1991, 1197.
- Staab, H. A.; Polenski, B. Liebigs Ann. Chem. 1962, 655, 95. https://doi.org/10.1002/jlac.19626550114
- Effenbergger, F.; Muck, A. O.; Bessey, E. Chem. Ber. 1980, 113,2086. https://doi.org/10.1002/cber.19801130605
- Shirini, F.; Zolfigol, M. A.; Mallakpour, B.; Mallakpour, S. E.;Hajipour, A. R. Aust. J. Chem. 2001, 54, 405. https://doi.org/10.1071/CH01104
- Shirini, F.; Zolfigol, M. A.; Mallakpour, B.; Mallakpour, S. E.;Hajipour, A. R.; Mohammadpour-Baltork, I. Tetrahedron Lett.2002, 43, 1555. https://doi.org/10.1016/S0040-4039(02)00007-2
- Chandra, K. L.; Saravanan, P.; Singh, R. K.; Singh, V. K.Tetrahedron 2002, 58, 1369. https://doi.org/10.1016/S0040-4020(01)01229-7
- Ram, R. N.; Meher, N. K. Tetrahedron 2002, 58, 2997. https://doi.org/10.1016/S0040-4020(02)00185-0
- Aldrich Catalogue, Handbook of Fine Chemicals; 1990-1991.
- CRC Handbook of Chemistry and Physics, 54th ed.; CRC Press:Boca Raton, 1973.
- Bilestine Handbook of Organic Chemistry, 4th ed.; Springer:Berlin, 1998.
- Vogel, A. I. Quqntitative Inorganic Analysis; Longman: London,1972; pp 462, 472, 792.
Cited by
- /KI in Nonaqueous Solution vol.36, pp.1, 2006, https://doi.org/10.1080/00397910500330577
- Silica Triflate as an Efficient Reagent for the Chemoselective Formylation of Alcohols vol.182, pp.6, 2007, https://doi.org/10.1080/10426500601160710
- Pyrazinium Di(hydrogen sulfate) as a Novel, Highly Efficient and Homogeneous Catalyst for the Condensation of Enolizable Ketones with Aldehydes, Acetonitrile and Acetyl Chloride vol.59, pp.2, 2012, https://doi.org/10.1002/jccs.201100383
- H: An Efficient Catalyst for Acylation of Sulfonamides Amines, Alcohols, and Phenols under Solvent-Free Conditions vol.2013, pp.2090-5157, 2013, https://doi.org/10.1155/2013/951749
- Aluminum hydrogen sulfate [Al(HSO4)3] as an efficient catalyst for the preparation of thioacetals vol.39, pp.6, 2013, https://doi.org/10.1007/s11164-012-0802-8
- Metal Hydrogen Sulfates Catalyzed Methoxymethylation of Alcohols under Solvent-Free Conditions vol.54, pp.4, 2013, https://doi.org/10.1002/jccs.200700153
- -Butyldimethyl Silylations of Aliphatic and Aromatic Alcohols in Solution and under Solvent-free Conditions vol.61, pp.8, 2014, https://doi.org/10.1002/jccs.201300586
- Al(HSO4)3 Catalyzed Acetylation and Formylation of Alcohols. vol.35, pp.17, 2004, https://doi.org/10.1002/chin.200417059
- Chamosite, a naturally occurring clay as a versatile catalyst for various organic transformations vol.45, pp.03, 2010, https://doi.org/10.1180/claymin.2010.045.3.281
- Reaction of carbohydrates with Vilsmeier reagent: a tandem selective chloro O-formylation of sugars vol.7, pp.7, 2009, https://doi.org/10.1039/b900026g
- Al(HSO 4 ) 3 as an Efficient Reagent for the Selective Trimethylsilylation of Primary Alcohols Under Solvent-Free Conditions vol.180, pp.10, 2003, https://doi.org/10.1080/104265090920930
- Selective Oxidative Deprotection of Trimethylsilyl Ethers in Solution and under a Solvent Free Condition vol.26, pp.11, 2003, https://doi.org/10.5012/bkcs.2005.26.11.1833
- Silica Sulfuric Acid and Al(HSO4)3: As Efficient Catalysts for the Formylation of Alcohols by Using Ethyl Formate under Heterogeneous Conditions vol.55, pp.4, 2003, https://doi.org/10.1002/jccs.200800132
- Polyaniline nanofiber supported FeCl3: An efficient and reusable heterogeneous catalyst for the acylation of alcohols and amines with acetic acid vol.302, pp.1, 2003, https://doi.org/10.1016/j.molcata.2008.12.011
- Vanadium Hydrogen Sulfate Catalyzed Solvent-Free Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones and Bis-(indolyl) methanes vol.31, pp.6, 2003, https://doi.org/10.5012/bkcs.2010.31.6.1715
- Production of biodiesel from mixed waste vegetable oil using an aluminium hydrogen sulphate as a heterogeneous acid catalyst vol.102, pp.15, 2003, https://doi.org/10.1016/j.biortech.2011.04.100
- A Mild and Highly Efficient Method for the Preparation of Silyl Ethers using Fe(HSO4)3/Et3N by Chlorosilanes vol.59, pp.11, 2003, https://doi.org/10.1002/jccs.201100701
- SYNTHESIS OF BETULIN DIFORMATE AND ALLOBETULIN FORMATE DIRECTLY FROM OUTER BIRCH BARK vol.2019, pp.1, 2003, https://doi.org/10.14258/jcprm.2019014682
- Novel Method for O-Acetylation of Cholesterol, Allobetulin, and Betulin vol.55, pp.3, 2003, https://doi.org/10.1007/s10600-019-02720-9
- Recent advances in O-formylation of alcohols and phenols using efficient catalysts in eco-friendly media vol.50, pp.14, 2003, https://doi.org/10.1080/00397911.2020.1744015