Highly efficient and versatile acetylation of alcohols catalyzed by cerium(III) triflate

[1]  G. Sindona,et al.  Simple and efficient chemoselective mild deprotection of acetals and ketals using cerium(III) triflate. , 2002, The Journal of organic chemistry.

[2]  A. Tagarelli,et al.  Deprotection of t-butyldimethylsilyl ethers promoted by cerium(IV) triflate , 2002 .

[3]  J. Baker,et al.  A one-step procedure for the monoacylation of symmetrical 1,2-diols. , 2002, The Journal of organic chemistry.

[4]  A. Loupy,et al.  Ac2O-Py/basic alumina as a versatile reagent for acetylations in solvent-free conditions under microwave irradiation , 2002 .

[5]  A. V. Ramaswamy,et al.  Acylation of alcohols, thiols and amines with carboxylic acids catalyzed by yttria–zirconia-based Lewis acid , 2002 .

[6]  Rajesh P. Singh,et al.  Lewis acid catalyzed acylation reactions: scope and limitations , 2002 .

[7]  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.

[8]  K. Babu,et al.  KF–Al 2 O 3 is an efficient solid support reagent for the acetylation of amines, alcohols, and phenols. Impeding effect of solvent on the reaction rate , 2001 .

[9]  E. Marcantoni,et al.  Cerium-Mediated Deprotection of Substituted Allyl Ethers , 2001 .

[10]  Orita,et al.  Highly Efficient and Versatile Acylation of Alcohols with Bi(OTf)(3) as Catalyst. , 2000, Angewandte Chemie.

[11]  S. V. Pansare,et al.  Magnesium Bromide Catalysed Acylation of Alcohols , 2000 .

[12]  C. Frost,et al.  INDIUM TRIFLATE : AN EFFICIENT CATALYST FOR ACYLATION REACTIONS , 1999 .

[13]  K. Ohashi,et al.  Remarkably Fast Acylation of Alcohols with Benzoyl Chloride Promoted by TMEDA , 1999 .

[14]  Anna Cappa,et al.  A Simple Method for the Selective Deprotection of p-Methoxybenzyl Ethers by Cerium(III) Chloride Heptahydrate and Sodium Iodide. , 1999, The Journal of organic chemistry.

[15]  V. Singh,et al.  AN EFFICIENT METHOD FOR ACYLATION REACTIONS , 1999 .

[16]  M. Kantam,et al.  Vanadyl(IV) acetate, a new reusable catalyst for acetylation of alcohols , 1999 .

[17]  Y. Hamada,et al.  Mild and practical acylation of alcohols with esters or acetic anhydride under distannoxane catalysis , 1999 .

[18]  Hong Zhao,et al.  General Procedure for Acylation of 3° Alcohols: Scandium Triflate/DMAP Reagent , 1998 .

[19]  Tong‐Shuang Li,et al.  Sulfamic Acid Catalysed Acetylation of Alcohols and Phenols with Acetic Anhydride , 1998 .

[20]  P. Ciuffreda,et al.  Lipase-catalysed chemoselective monoacetylation of hydroxyalkylphenols and chemoselective removal of a single acetyl group from their diacetates , 1998 .

[21]  S. Carloni,et al.  Zeolite HSZ-360 as a new reusable catalyst for the direct acetylation of alcohols and phenols under solventless conditions , 1998 .

[22]  H. W. Scheeren,et al.  Lanthanide trifluoromethanesulfonate catalysed selective acylation of 10-deacetylbaccatin III , 1998 .

[23]  Toshio Suzuki,et al.  Acetylation and formylation of alcohols with triphenylphosphine and carbon tetrabromide in ethyl acetate or ethyl formate , 1998 .

[24]  S. Chandrasekhar,et al.  Acylation of alcohols with acetic anhydride catalyzed by TaCl5: Some implications in kinetic resolution , 1998 .

[25]  P. Procopiou,et al.  An Extremely Powerful Acylation Reaction of Alcohols with Acid Anhydrides Catalyzed by Trimethylsilyl Trifluoromethanesulfonate , 1998 .

[26]  E. Marcantoni,et al.  A mild, efficient, and selective method for the desilylation of more common trialkylsilyl ethers by cerium(III) chloride heptahydrate and sodium iodide in acetonitrile , 1998 .

[27]  G. Breton Selective Monoacetylation of Unsymmetrical Diols Catalyzed by Silica Gel-Supported Sodium Hydrogen Sulfate , 1997 .

[28]  R. Field,et al.  Iodine: A versatile reagent in carbohydrate chemistry IV. Per-O-acetylation, regioselective acylation and acetolysis , 1997 .

[29]  F. Nobili,et al.  Cerium (III) Chloride, a Novel Reagent for Nonaqueous Selective Conversion of Dioxolanes to Carbonyl Compounds , 1997 .

[30]  S. L. Kurtz,et al.  Acetylation of unsymmetrical diols in the presence of Al2O3 , 1997 .

[31]  T. Ding,et al.  Montmorillonite K-10 and KSF as remarkable acetylation catalysts , 1997 .

[32]  N. Deka,et al.  Iodine as an Acetyl Transfer Catalyst , 1997 .

[33]  A. Barrett,et al.  Scandium(III) or lanthanide(III) triflates as recyclable catalystsfor the direct acetylation of alcohols with acetic acid , 1997 .

[34]  S. Yamada,et al.  Twisted Amides as Selective Acylating Agents for Hydroxyl Groups under Neutral Conditions: Models for Activated Peptides during Enzymatic Acyl Transfer Reaction , 1996 .

[35]  O. Daugulis,et al.  Dual Activation in the Esterification of Hindered Alcohols with Anhydrides Using MgBr2 and a Tertiary Amine , 1996 .

[36]  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.

[37]  E. Vedejs,et al.  Enantioselective Acylations Catalyzed by Chiral Phosphines. , 1996, Journal of Organic Chemistry.

[38]  P. Procopiou,et al.  An extremely fast and efficient acylation reaction of alcohols with acid anhydrides in the presence of trimethylsilyl trifluoromethanesulfonate as catalyst , 1996 .

[39]  M. Kubota,et al.  SCANDIUM TRIFLUOROMETHANESULFONATE AS AN EXTREMELY ACTIVE ACYLATION CATALYST , 1995 .

[40]  M. J. Peterson,et al.  Tributylphosphine-catalyzed acylations of alcohols: Scope and related reactions , 1993 .

[41]  S. Diver,et al.  Tributylphosphine: a remarkable acylation catalyst , 1993 .

[42]  J. Iqbal,et al.  Cobalt(II) chloride catalyzed acylation of alcohols with acetic anhydride: scope and mechanism , 1992 .

[43]  E. Scriven 4-Dialkylaminopyridines: super acylation and alkylation catalysts , 1983 .

[44]  J. Barlow,et al.  The selective acetylation of primary alcohols in the presence of secondary alcohols in carbohydrates , 1982 .

[45]  G. Höfle,et al.  4‐Dialkylaminopyridines as Highly Active Acylation Catalysts. [New synthetic method (25)] , 1978 .

[46]  R. Zhdanov,et al.  Chemical Methods of Oligonucleotide Synthesis , 1975 .

[47]  G. Höfle,et al.  N,N‐Dimethyl‐4‐pyridinamine, a Very Effective Acylation Catalyst , 1969 .