Stripping off water at ambient temperature: direct atom-efficient acetal formation between aldehydes and diols catalyzed by water-tolerant and recoverable vanadyl triflate.

[reaction: see text]. Aromatic aldehydes can be readily protected as acetals with 1,2- and 1,3-diols by using vanadyl triflate as a catalyst in CH(3)CN at ambient temperature. Carbohydrate-based 1,2- and 1,3-diols can similarly be protected in good to excellent yields. The catalyst can be readily recovered from the aqueous layer. In combination with vanadyl triflate-catalyzed sequential regioselective, reductive acetal opening and chemoselective acylations, the title method allows for differential functionalization of all four hydroxyl units in a given glucopyranoside.

[1]  Chien-Tien Chen,et al.  Diethylene glycol ether-linked 3,4,5-trihydroxybenzamides as triply branched dendritic anchors to CdSe/ZnS core/shell type nanoparticles: potential hydrophilic fluorescent probes. , 2005, Chemical communications.

[2]  Chien-Tien Chen,et al.  Nucleophilic acyl substitutions of anhydrides with protic nucleophiles catalyzed by amphoteric, oxomolybdenum species. , 2005, The Journal of organic chemistry.

[3]  Chien-Tien Chen,et al.  Nucleophilic acyl substitutions of esters with protic nucleophiles mediated by amphoteric, oxotitanium, and vanadyl species. , 2005, The Journal of organic chemistry.

[4]  P. Chou,et al.  Site-selective DNA photocleavage involving unusual photoinitiated tautomerization of chiral tridentate vanadyl(V) complexes derived from N-salicylidene alpha-amino acids. , 2004, Organic letters.

[5]  A. Wei,et al.  Temperature-controlled regioselectivity in the reductive cleavage of p-methoxybenzylidene acetals. , 2004, The Journal of organic chemistry.

[6]  Jinq-chyi Lee,et al.  Synthesis of heparin oligosaccharides. , 2004, Journal of the American Chemical Society.

[7]  W. Hakamata,et al.  Convenient preparation of cyclic acetals, using diols, TMS-source, and a catalytic amount of TMSOTf. , 2003, The Journal of organic chemistry.

[8]  Chien-Tien Chen,et al.  Catalytic asymmetric oxidative couplings of 2-naphthols by tridentate N-ketopinidene-based vanadyl dicarboxylates. , 2002, Organic letters.

[9]  R. Mohan,et al.  A simple and versatile method for the synthesis of acetals from aldehydes and ketones using bismuth triflate. , 2002, The Journal of organic chemistry.

[10]  S. Hung,et al.  Metal trifluoromethanesulfonate-catalyzed regioselective borane-reductive ring opening of benzylidene acetals: a concise synthesis of 1,4-dideoxy-1,4-imino-L-xylitol. , 2002, Organic letters.

[11]  C. Liu,et al.  Catalytic nucleophilic acyl substitution of anhydrides by amphoteric vanadyl triflate. , 2001, Organic letters.

[12]  F. P. Boulineau,et al.  Stereoselective synthesis of [13C]methyl 2-[15N]amino-2-deoxy-beta-D-glucopyranoside derivatives. , 2001, Carbohydrate research.

[13]  Xiao‐Feng Wang,et al.  An Efficient and Convenient Method for Preparation of 2,2-Disubstituted and 2-Monosubstituted 1,3-Benzodioxoles from Ketones and Aldehydes with Catechol Catalysed by ZrO2/SO42- , 2001 .

[14]  Y. H. Liu,et al.  Catalytic asymmetric coupling of 2-naphthols by chiral tridentate oxovanadium (IV) complexes. , 2001, Organic letters.

[15]  F. D’Andrea,et al.  Concise synthesis of 1-deoxy-4-O-β-d-galactopyranosyl-d-nojirimycin avoiding a glycosylation step , 2001 .

[16]  B. Karimi,et al.  Efficient and Chemoselective Conversion of Carbonyl Compounds to 1,3-Dioxanes Catalyzed with N-Bromosuccinimide under Almost Neutral Reaction Conditions , 1999 .

[17]  B. Karimi,et al.  N-Bromosuccinimide (NBS) as a Powerful and Chemoselective Catalyst for Acetalization of Carbonyl Compounds under almost Neutral Reaction Conditions , 1999 .

[18]  B. Karimi,et al.  Tungsten Hexachloride (WCl6), A Highly Efficient and Chemoselective Catalyst for Acetalization of Carbonyl Compounds , 1999 .

[19]  Chien-Tien Chen,et al.  Oxovanadium(IV) Complex-mediated Catalysis in Mukaiyama-type Aldol Additions , 1999 .

[20]  B. Karimi,et al.  ZIRCONIUM TETRACHLORIDE (ZRCL4) CATALYZED HIGHLY CHEMOSELECTIVE AND EFFICIENT ACETALIZATION OF CARBONYL COMPOUNDS , 1999 .

[21]  N. Pastori,et al.  Efficient acetalisation of aldehydes catalyzed by titanium tetrachloride in a basic medium , 1998 .

[22]  Chi‐Huey Wong,et al.  ASSEMBLY OF OLIGOSACCHARIDE LIBRARIES WITH A DESIGNED BUILDING BLOCK AND AN EFFICIENT ORTHOGONAL PROTECTION-DEPROTECTION STRATEGY , 1998 .

[23]  T. Chan,et al.  Borane/Bu2BOTf: A mild reagent for the regioselective reductive ring opening of benzylidene acetals in carbohydrates , 1998 .

[24]  H. Waldmann,et al.  PROTECTING GROUP STRATEGIES IN ORGANIC SYNTHESIS , 1996 .

[25]  M. Kubota,et al.  SCANDIUM TRIFLUOROMETHANESULFONIMIDE AND SCANDIUM TRIFLUOROMETHANESULFONATE AS EXTREMELY ACTIVE ACETALIZATION CATALYSTS , 1996 .

[26]  R. Mahrwald A Simple Procedure for the Catalytic Acetalization of Aldehydes , 1994 .

[27]  W. Scott,et al.  1,3-Dioxolane formation via Lewis acid-catalyzed reaction of ketones with oxiranes , 1993 .

[28]  P. Konradsson,et al.  Iodonium promoted reactions of disarmed thioglycosides , 1990 .

[29]  J. H. Boom,et al.  An efficient thioglycoside-mediated formation of α-glycosidic linkages promoted by iodonium dicollidine perchlorate , 1990 .

[30]  P. Garegg,et al.  A novel promoter for the efficient construction of 1,2-trans linkages in glycoside synthesis, using thioglycosides as glycosyl donors , 1986 .

[31]  D. Seebach,et al.  EPC Syntheses with C, C Bond Formation via Acetals and Enamines , 1986 .

[32]  G. A. Berchtold,et al.  TOTAL SYNTHESIS OF RACEMIC CHORISMIC ACID AND (-)-5-ENOLPYRUVYLSHIKIMIC ACID (“COMPOUND Z1”) , 1983 .

[33]  C. Copeland,et al.  The conversion of some carbohydrate diols into cyclic carbonates and thiocarbonates by means of N-dichloromethylene-N,N-dimethylammonium chloride (Viehe's salt) , 1982 .

[34]  F. Meskens Methods for the Preparation of Acetals from Alcohols or Oxiranes and Carbonyl Compounds , 1981 .

[35]  Masaaki Suzuki,et al.  A facile procedure for acetalization under aprotic conditions , 1980 .

[36]  J. Luche,et al.  Lanthanoids in organic synthesis. 4. Selective ketalization and reduction of carbonyl groups , 1979 .

[37]  T. E. Goodwin,et al.  4-Formyl-2-cyclohexenone Derivatives , 1978 .

[38]  J. J. Kibby,et al.  Chiral benzylidene derivatives of glycerol , 1976 .

[39]  S. Dev,et al.  Amberlyst-15, a Superior Catalyst for the Preparation of Enol Ethers and Acetals , 1974 .

[40]  N. Andersen,et al.  Methods for Interconverting Aldehydes and Acetals , 1973 .

[41]  K. Byrne,et al.  Relative reactivities of cycloalkanone dimethyl ketals to hydrogenolysis by dichloroaluminum hydride , 1970 .

[42]  J. S. Hunt,et al.  788. Studies in the synthesis of cortisone. Part III. The degradation of the ergosterol side chain , 1953 .