Zinc perchlorate hexahydrate [Zn(ClO4)2·6H2O] as acylation catalyst for poor nucleophilic phenols, alcohols and amines: Scope and limitations
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[1] S. Chankeshwara,et al. HClO4-SiO2 as a new, highly efficient, inexpensive and reusable catalyst for N-tert-butoxycarbonylation of amines. , 2006, Organic & biomolecular chemistry.
[2] A. Chakraborti,et al. Magnesium bistrifluoromethanesulfonimide as a new and efficient acylation catalyst. , 2006, The Journal of organic chemistry.
[3] J. S. Carey,et al. Analysis of the reactions used for the preparation of drug candidate molecules. , 2006, Organic & biomolecular chemistry.
[4] A. Chakraborti,et al. Zinc(II) perchlorate as a new and highly efficient catalyst for formation of aldehyde 1,1-diacetate at room temperature and under solvent-free conditions , 2006 .
[5] Eric V. Anslyn,et al. Modern Physical Organic Chemistry , 2005 .
[6] M. Salavati‐Niasari,et al. Manganese(III) bis(2-hydroxyanil)acetylacetonato complex as effective catalyst for acylation of alcohols, amines and phenols with acetic anhydride , 2005 .
[7] Chien-Tien Chen,et al. Nucleophilic acyl substitutions of anhydrides with protic nucleophiles catalyzed by amphoteric, oxomolybdenum species. , 2005, The Journal of organic chemistry.
[8] A. Chakraborti,et al. Magnesium perchlorate as an efficient catalyst for the synthesis of imines and phenylhydrazones , 2004 .
[9] G. Sindona,et al. Erbium(III) Triflate as an Extremely Active Acylation Catalyst , 2004 .
[10] A. Chakraborty,et al. Facile catalyzed acylation of heteroatoms using BiCl3 generated in situ from the procatalyst BiOCl and acetyl chloride , 2004 .
[11] A. Chakraborti,et al. Zirconium(IV) Chloride as a New, Highly Efficient, and Reusable Catalyst for Acetylation of Phenols, Thiols, Amines, and Alcohols under Solvent-Free Conditions , 2004 .
[12] S. De. Ruthenium(III) chloride catalyzed acylation of alcohols, phenols, thiols, and amines , 2004 .
[13] V. Yadav,et al. Reactions on a solid surface. A simple, economical, and efficient acylation of alcohols and amines over Al2O3. , 2004, The Journal of organic chemistry.
[14] Raphael Dumeunier,et al. On the role of triflic acid in the metal triflate-catalysed acylation of alcohols , 2004 .
[15] A. Chakraborti,et al. Copper(II) Tetrafluoroborate-Catalyzed Acetylation of Phenols, Thiols, Alcohols, and Amines , 2003 .
[16] E. Marcantoni,et al. Zn(ClO4)2·6H2O as a Powerful Catalyst for a Practical Acylation of Alcohols with Acid Anhydrides , 2003 .
[17] A. Chakraborti,et al. Bismuth Oxide Perchlorate as a Highly Efficient Catalyst for Heteroatom Acylation Under Solvent-Free Conditions , 2003 .
[18] Shivani,et al. Electrostatic catalysis by ionic aggregates: scope and limitations of Mg(ClO4)2 as acylation catalyst , 2003 .
[19] A. Chakraborti,et al. Indium(III) chloride as a new, highly efficient, and versatile catalyst for acylation of phenols, thiols, alcohols, and amines , 2003 .
[20] R. Romeo,et al. Highly efficient and versatile acetylation of alcohols catalyzed by cerium(III) triflate , 2003 .
[21] A. Chakraborti,et al. Perchloric acid adsorbed on silica gel as a new, highly efficient, and versatile catalyst for acetylation of phenols, thiols, alcohols, and amines. , 2003, Chemical communications.
[22] B. Karimi,et al. Lithium trifluoromethanesulfonate (LiOTf) as a recyclable catalyst for highly efficient acetylation of alcohols and diacetylation of aldehydes under mild and neutral reaction conditions. , 2003, The Journal of organic chemistry.
[23] A. Chakraborti,et al. Fluoroboric acid adsorbed on silica gel as a new and efficient catalyst for acylation of phenols, thiols, alcohols, and amines , 2003 .
[24] N. Iranpoor,et al. Aluminium dodecatungstophosphate (AlPW12O40) as a highly efficient catalyst for the selective acetylation of -OH, -SH and -NH2 functional groups in the absence of solvent at room temperature. , 2003, Chemical communications.
[25] K. Ishihara,et al. Crucial role of the ligand of silyl Lewis acid in the Mukaiyama aldol reaction. , 2002, Chemical communications.
[26] D. Macfarlane,et al. Rapid, clean, and mild O-acetylation of alcohols and carbohydrates in an ionic liquid. , 2002, Chemical communications.
[27] Lalima Sharma,et al. Influence of hydrogen bonding in the activation of nucleophiles: PhSH-(catalytic) KF in N-methyl-2-pyrrolidone as an efficient protocol for selective cleavage of alkyl/aryl esters and aryl alkyl ethers under nonhydrolytic and neutral conditions. , 2002, The Journal of organic chemistry.
[28] Lalima Sharma,et al. Diphenyl disulfide and sodium in NMP as an efficient protocol for in situ generation of thiophenolate anion: selective deprotection of aryl alkyl ethers and alkyl/aryl esters under nonhydrolytic conditions. , 2002, The Journal of organic chemistry.
[29] Rajesh P. Singh,et al. Lewis acid catalyzed acylation reactions: scope and limitations , 2002 .
[30] A. Zwick,et al. A practical, cheap and environmentally friendly preparation of bismuth(III) trifluoromethanesulfonate , 2002 .
[31] A. Orita,et al. Highly powerful and practical acylation of alcohols with acid anhydride catalyzed by Bi(OTf)(3). , 2001, The Journal of organic chemistry.
[32] Upasana Sharma,et al. A mild and chemoselective method for deprotection of aryl acetates and benzoates under non-hydrolytic condition , 2001 .
[33] I. Mohammadpoor‐Baltork,et al. Bismuth(III) salts as convenient and efficient catalysts for the selective acetylation and benzoylation of alcohols and phenols , 2001 .
[34] R. Mohan,et al. A Simple and Practical Method for Large-Scale Acetylation of Alcohols and Diols Using Bismuth Triflate , 2001 .
[35] Orita,et al. Highly Efficient and Versatile Acylation of Alcohols with Bi(OTf)(3) as Catalyst. , 2000, Angewandte Chemie.
[36] C. Frost,et al. INDIUM TRIFLATE : AN EFFICIENT CATALYST FOR ACYLATION REACTIONS , 1999 .
[37] Lalima Sharma,et al. Selective Deprotection of Aryl Acetates, Benzoates, Pivalates, and Tosylates under Nonhydrolytic and Virtually Neutral Conditions† , 1999 .
[38] V. Singh,et al. AN EFFICIENT METHOD FOR ACYLATION REACTIONS , 1999 .
[39] J. Desmurs,et al. An efficient method for the preparation of bismuth(III) trifluoromethanesulfonate , 1999 .
[40] J. R. Hanson,et al. Protecting Groups in Organic Synthesis , 1999 .
[41] Hong Zhao,et al. General Procedure for Acylation of 3° Alcohols: Scandium Triflate/DMAP Reagent , 1998 .
[42] P. Procopiou,et al. An Extremely Powerful Acylation Reaction of Alcohols with Acid Anhydrides Catalyzed by Trimethylsilyl Trifluoromethanesulfonate , 1998 .
[43] Hisashi Yamamoto,et al. Scandium Trifluoromethanesulfonate as an Extremely Active Lewis Acid Catalyst in Acylation of Alcohols with Acid Anhydrides and Mixed Anhydrides. , 1996, The Journal of organic chemistry.
[44] Hisashi Yamamoto,et al. A New Scandium Complex as an Extremely Active Acylation Catalyst , 1996 .
[45] Yukihiro Motoyama,et al. Metal Bis(trifluoromethylsulfonyl)amides as Highly Efficient Lewis Acid Catalysts for Acylation Reactions , 1996 .
[46] M. Kubota,et al. SCANDIUM TRIFLUOROMETHANESULFONATE AS AN EXTREMELY ACTIVE ACYLATION CATALYST , 1995 .
[47] J. Foropoulos,et al. Synthesis, properties, and reactions of bis((trifluoromethyl)sulfonyl) imide, (CF3SO2)2NH , 1984 .
[48] James E. Huheey,et al. Inorganic chemistry; principles of structure and reactivity , 1972 .
[49] S. A. Buckler. Autoxidation of Trialkylphosphines , 1962 .
[50] V. P. Vasil’ev,et al. Instability Constants of Complex Compounds , 1960 .