Stereocontrolled Photoinduced Glycosylation Using an Aryl Thiourea as an Organo photoacid.

Photoinduced glycosylation of alcohols with α-glucosyl trichloroacetimidates, using aryl urea and thioureas as organo photoacids, was examined under long wavelength UV (ultraviolet) irradiation. The results show, for the first time, that such glycosylations proceed effectively to give the corresponding glycosides in high yields. In addition, high β-stereoselectivity was obtained under high concentration conditions, whereas high α-stereoselectivity was realized under low concentration conditions.

[1]  De‐Cai Xiong,et al.  Photoinduced C-S Bond Cleavage of Thioglycosides and Glycosylation. , 2015, Organic letters.

[2]  Aaron B. Beeler,et al.  [2+2] Photocycloaddition of Cinnamates in Flow and Development of a Thiourea Catalyst. , 2015, Angewandte Chemie.

[3]  Chun‐Jiang Wang,et al.  Recent advances in asymmetric organocatalysis mediated by bifunctional amine-thioureas bearing multiple hydrogen-bonding donors. , 2015, Chemical communications.

[4]  D. Takahashi,et al.  Photo-induced glycosylation using reusable organophotoacids. , 2014, Chemical communications.

[5]  S. Jockusch,et al.  Enantioselective organo-photocatalysis mediated by atropisomeric thiourea derivatives. , 2014, Angewandte Chemie.

[6]  Clay S. Bennett,et al.  An Air- and Water-Stable Iodonium Salt Promoter for Facile Thioglycoside Activation , 2014, Organic letters.

[7]  Amit Kumar,et al.  Cooperative catalysis in glycosidation reactions with O-glycosyl trichloroacetimidates as glycosyl donors. , 2013, Angewandte Chemie.

[8]  D. Takahashi,et al.  Light-induced O-glycosylation of unprotected deoxythioglycosyl donors. , 2013, Organic & biomolecular chemistry.

[9]  Clay S. Bennett,et al.  Selective synthesis of 1,2-cis-α-glycosides without directing groups. Application to iterative oligosaccharide synthesis. , 2013, Organic letters.

[10]  A. Bowers,et al.  Visible light mediated activation and O-glycosylation of thioglycosides. , 2013, Organic letters.

[11]  D. Coe,et al.  α-Selective organocatalytic synthesis of 2-deoxygalactosides. , 2012, Angewandte Chemie.

[12]  E. Jacobsen,et al.  Thiourea-catalysed ring opening of episulfonium ions with indole derivatives by means of stabilising, non-covalent interactions , 2012, Nature Chemistry.

[13]  Jennifer J. Becker,et al.  A photoflow reactor for the continuous photoredox-mediated synthesis of C-glycoamino acids and C-glycolipids. , 2012, Angewandte Chemie.

[14]  P. Schreiner,et al.  (Thio)urea organocatalyst equilibrium acidities in DMSO. , 2012, Organic letters.

[15]  P. Schreiner,et al.  Cooperative thiourea-Brønsted acid organocatalysis: enantioselective cyanosilylation of aldehydes with TMSCN. , 2011, The Journal of organic chemistry.

[16]  K. K. Mong,et al.  Neighboring-group participation by C-2 ether functions in glycosylations directed by nitrile solvents. , 2011, Chemistry.

[17]  D. Crich,et al.  Photoinitiated Glycosylation at 350 nm , 2011 .

[18]  Jennifer J. Becker,et al.  Investigating the rate of photoreductive glucosyl radical generation. , 2011, Organic letters.

[19]  Jennifer J. Becker,et al.  Intermolecular addition of glycosyl halides to alkenes mediated by visible light. , 2010, Angewandte Chemie.

[20]  Y. Tao,et al.  Asymmetric Cooperative Catalysis of Strong Brønsted Acid–Promoted Reactions Using Chiral Ureas , 2010, Science.

[21]  H. Deng,et al.  Organocatalytic Three‐Component Reactions of Pyruvate, Aldehyde and Aniline by Hydrogen‐Bonding Catalysts , 2008 .

[22]  A. Demchenko Handbook of Chemical Glycosylation , 2008 .

[23]  A. Demchenko Handbook of chemical glycosylation : advances in stereoselectivity and therapeutic relevance , 2008 .

[24]  C. Biliaderis,et al.  Functional Food Carbohydrates , 2006 .

[25]  H. Imagawa,et al.  Hg(OTf)2-catalyzed glycosylation using alkynoate as the leaving group , 2006 .

[26]  Yong Tang,et al.  Pyrrolidine-thiourea as a bifunctional organocatalyst: highly enantioselective Michael addition of cyclohexanone to nitroolefins. , 2006, Organic letters.

[27]  Raquel P. Herrera,et al.  Catalytic enantioselective Friedel-Crafts alkylation of indoles with nitroalkenes by using a simple thiourea organocatalyst. , 2005, Angewandte Chemie.

[28]  Y. Takemoto,et al.  Enantio- and diastereoselective Michael reaction of 1,3-dicarbonyl compounds to nitroolefins catalyzed by a bifunctional thiourea. , 2005, Journal of the American Chemical Society.

[29]  Y. Takemoto,et al.  Enantioselective Michael reaction of malonates to nitroolefins catalyzed by bifunctional organocatalysts. , 2003, Journal of the American Chemical Society.

[30]  A. Demchenko Stereoselective Chemical 1,2-cis O-Glycosylation: From ‘Sugar Ray’ to Modern Techniques of the 21st Century , 2003 .

[31]  P. Schreiner,et al.  Metal-free, noncovalent catalysis of diels-alder reactions by neutral hydrogen bond donors in organic solvents and in water. , 2003, Chemistry.

[32]  G. Hart,et al.  Carbohydrates in chemistry and biology , 2000 .

[33]  M. Fagnoni,et al.  Environment-friendly organic synthesis. The photochemical approach , 2000 .

[34]  K. Takeuchi,et al.  Activation of selenoglycosides by photoinduced electron transfer , 1996 .

[35]  M. Shibasaki,et al.  A NEW GLYCOSYLATION PROCEDURE UTILIZING RARE EARTH SALTS AND GLYCOSYL FLUORIDES, WITH OR WITHOUT THE REQUIREMENT OF LEWIS ACIDS , 1995 .

[36]  J. Haubrich,et al.  Photoexcited Proton Transfer from Enhanced Photoacids , 1994 .

[37]  M. A. Clarke,et al.  Photoinduced generation of glucosyl cations from thioglycosides , 1990 .

[38]  M. Hayashi,et al.  Glycosylation using glucopyranosyl fluorides and silicon-based catalysts. Solvent dependency of the stereoselection , 1984 .