Stereocontrolled Photoinduced Glycosylation Using an Aryl Thiourea as an Organo photoacid.
暂无分享,去创建一个
[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 .