Pure and Applied Chemistry

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• Dang Hester, Cox Nick, Lalic Gojko: Copper-Catalyzed Reduction of Alkyl Triflates and Iodides: An Efficient Method for the Deoxygenation of Primary and Secondary Alcohols. Angew. Chem. 2014, 126, 771. <http://dx.doi.org/10.1002/ange.201307697>
• Dang Hester, Cox Nick, Lalic Gojko: Copper-Catalyzed Reduction of Alkyl Triflates and Iodides: An Efficient Method for the Deoxygenation of Primary and Secondary Alcohols. Angew. Chem. Int. Ed. 2014, 53, 752. <http://dx.doi.org/10.1002/anie.201307697>
• Wei Yawen, Wang Chao, Jiang Xue, Xue Dong, Liu Zhao-Tie, Xiao Jianliang: Catalyst-free transformation of levulinic acid into pyrrolidinones with formic acid. Green Chem. 2014, 16, 1093. <http://dx.doi.org/10.1039/c3gc42125b>
• Brust Andreas, Cuny Eckehard: Reducing disaccharides and their 1,2-dicarbonyl intermediates as building blocks for nitrogen heterocycles. RSC Adv. 2014, 4, 5759. <http://dx.doi.org/10.1039/c3ra47349j>
• Kundu Sabuj, Choi Jongwook, Wang David Y., Choliy Yuriy, Emge Thomas J., Krogh-Jespersen Karsten, Goldman Alan S.: Cleavage of Ether, Ester, and Tosylate C(sp3)–O Bonds by an Iridium Complex, Initiated by Oxidative Addition of C–H Bonds. Experimental and Computational Studies. J. Am. Chem. Soc. 2013, 135, 5127. <http://dx.doi.org/10.1021/ja312464b>
• Wei Yawen, Wang Chao, Jiang Xue, Xue Dong, Li Jia, Xiao Jianliang: Highly efficient transformation of levulinic acid into pyrrolidinones by iridium catalysed transfer hydrogenation. Chem. Commun. 2013, 49, 5408. <http://dx.doi.org/10.1039/c3cc41661e>
• Brust Andreas, Lichtenthaler Frieder W.: Facile conversion of glycosyloxymethyl-furfural into γ-keto-carboxylic acid building blocks towards a sustainable chemical industry. Green Chem. 2013, 15, 1368. <http://dx.doi.org/10.1039/c3gc40185e>
• Brust Andreas, Cuny Eckehard: Conversion of reducing carbohydrates into hydrophilic substituted imidazoles. Green Chem. 2013, 15, 2993. <http://dx.doi.org/10.1039/c3gc41203b>
• Murru Siva, Nicholas Kenneth M., Srivastava Radhey S.: Ruthenium (II) sulfoxides-catalyzed hydrogenolysis of glycols and epoxides. Journal of Molecular Catalysis A: Chemical 2012, 363-364, 460. <http://dx.doi.org/10.1016/j.molcata.2012.07.025>
• Stanowski Sylvain, Nicholas Kenneth M., Srivastava Radhey S.: [Cp*Ru(CO)₂]₂-Catalyzed Hydrodeoxygenation and Hydrocracking of Diols and Epoxides. Organomettalics 2012, 31, 515. <http://dx.doi.org/10.1021/om200447z>
• Li Li, Korányi Tamás I., Sels Bert F., Pescarmona Paolo P.: Highly-efficient conversion of glycerol to solketal over heterogeneous Lewis acid catalysts. Green Chem. 2012, 14, 1611. <http://dx.doi.org/10.1039/c2gc16619d>
• Daudé David, Remaud-Siméon Magali, André Isabelle: Sucrose analogs: an attractive (bio)source for glycodiversification. Nat. Prod. Rep. 2012, 29, 945. <http://dx.doi.org/10.1039/c2np20054f>
• Ruß Carolin, Luff Claudia, Begli Alireza Haji, Koenig Burkhard: Solvent-Free Preparation of 5-(α-D-Glucosyloxymethyl)furfural from Isomaltulose–Choline Chloride Melts. Synthetic Communications 2012, 42, 3112. <http://dx.doi.org/10.1080/00397911.2011.576375>
• Zebiri Ilhem, Balieu Sébastien, Guilleret Arnaud, Reynaud Romain, Haudrechy Arnaud: The Chemistry of L-Sorbose. Eur J Org Chem 2011, 2011, 2905. <http://dx.doi.org/10.1002/ejoc.201001578>
• Ramstadius Clinton, Träff Annika M., Krumlinde Patrik, Bäckvall Jan-E., Cumpstey Ian: Ruthenium-Catalysed Epimerisation of Carbohydrate Alcohols as a Method to Determine the Equilibria for Epimer Interconversion in Hexopyranosides. Eur J Org Chem 2011, 2011, 4455. <http://dx.doi.org/10.1002/ejoc.201100504>
• Boklund Mikael, Cumpstey Ian, Ramstadius Clinton: Conversion of fructose into a building block for the synthesis of carbocyclic mannose mimics. Tet Asymm 2011, 22, 399. <http://dx.doi.org/10.1016/j.tetasy.2011.02.013>
• Cumpstey Ian, Agrawal Santosh, Borbas K. Eszter, Martín-Matute Belén: Iridium-catalysed condensation of alcohols and amines as a method for aminosugar synthesis. Chem Commun 2011, 47, 7827. <http://dx.doi.org/10.1039/c1cc12800k>
• Barros M. Teresa, Petrova Krasimira T., Correia-da-Silva Paula, Potewar Taterao M.: Library of mild and economic protocols for the selective derivatization of sucrose under microwave irradiation. Green Chem 2011, 13, 1897. <http://dx.doi.org/10.1039/c1gc15228a>
• Schlaf Marcel, Ghosh Prasenjit, Fagan Paul J., Hauptman Elisabeth, Bullock R. Morris: Catalytic Deoxygenation of 1,2-Propanediol to Give n-Propanol. Adv Synth Catal 2009, 351, 789. <http://dx.doi.org/10.1002/adsc.200800685>
• Dimitratos Nikolaos, Lopez-Sanchez Jose Antonio, Hutchings Graham J.: Green Catalysis with Alternative Feedstocks. Top Catal 2009, 52, 258. <http://dx.doi.org/10.1007/s11244-008-9162-4>
• Prati Laura, Spontoni Paolo, Gaiassi Aureliano: From Renewable to Fine Chemicals Through Selective Oxidation: The Case of Glycerol. Top Catal 2009, 52, 288. <http://dx.doi.org/10.1007/s11244-008-9165-1>
• Villa Alberto, Tessonnier Jean-Philippe, Majoulet Olivier, Su Dang Sheng, Schlögl Robert: Amino-functionalized carbon nanotubes as solid basic catalysts for the transesterification of triglycerides. Chem Commun 2009, 4405. <http://dx.doi.org/10.1039/b906123a>
• Yin An-Yuan, Guo Xiu-Ying, Dai Wei-Lin, Fan Kang-Nian: The synthesis of propylene glycol and ethylene glycol from glycerol using Raney Ni as a versatile catalyst. Green Chem 2009, 11, 1514. <http://dx.doi.org/10.1039/b913395j>
• Lima Sérgio, Dias Ana S., Lin Zhi, Brandão Paula, Ferreira Paula, Pillinger Martyn, Rocha João, Calvino-Casilda Vanesa, Valente Anabela A.: Isomerization of d-glucose to d-fructose over metallosilicate solid bases. CATAL A GENERAL 2008, 339, 21. <http://dx.doi.org/10.1016/j.apcata.2007.12.030>
• Cumpstey Ian, Gehrke Sebastian, Erfan Sayeh, Cribiu Riccardo: Studies on the synthesis of valienamine and 1-epi-valienamine starting from d-glucose or l-sorbose. Carbohydrates Research 2008, 343, 1675. <http://dx.doi.org/10.1016/j.carres.2008.04.010>
• Cribiù Riccardo, Cumpstey Ian: Stereospecific debenzylative cycloetherification of carbohydrate-derived allylic alcohols, ethers and esters to form vinyl C-furanosides. Chem Commun 2008, 1246. <http://dx.doi.org/10.1039/b718060h>
• El Ashry El Sayed H., Atta Kamal F., Aboul‐Ela Salah, Beldi Razika: MAOS of Quinoxalines, Conjugated Pyrazolylquinoxalines and Fused Pyrazoloquinoxalines from l‐Ascorbic and d‐Isoascorbic Acid. J Carbohydr Chem 2007, 26, 1. <http://dx.doi.org/10.1080/07328300701252359>
• El Ashry E. S. H., Atta K. F., Aboul‐Ela S., Beldi R.: MAOS of Sugar Phenylosazones and their Derived Pyrazoles and Triazoles. J Carbohydr Chem 2007, 26, 429. <http://dx.doi.org/10.1080/07328300701787164>
• Schlaf Marcel: Selective deoxygenation of sugar polyols to ?,?-diols and other oxygen content reduced materials?a new challenge to homogeneous ionic hydrogenation and hydrogenolysis catalysis. Dalton Trans 2006, 4645. <http://dx.doi.org/10.1039/b608007c>
• Lucia Lucian A, Argyropoulos Dimitris S, Adamopoulos Lambrini, Gaspar Armindo R: Chemicals and energy from biomass. Can J Chem 2006, 84, 960. <http://dx.doi.org/10.1139/v06-117>
• Roussel Myriam, Benvegnu Thierry, Lognoné Vincent, Le Deit Hervé, Soutrel Isabelle, Laurent Isabelle, Plusquellec Daniel: Synthesis and Physico-Chemical Properties of Novel Biocompatible AlkylD-Mannopyranosiduronate Surfactants Derived from Alginate. Eur J Org Chem 2005, 2005, 3085. <http://dx.doi.org/10.1002/ejoc.200500026>
• Badorrey Ramón, Cativiela Carlos, Dı́az-de-Villegas Marı́a D, Gálvez José A: Highly convergent stereoselective synthesis of chiral key intermediates in the synthesis of Palinavir from imines derived from l-glyceraldehyde. Tetrahedron 2002, 58, 341. <http://dx.doi.org/10.1016/S0040-4020(01)01152-8>
• Schlaf Marcel, Ghosh Prasenjit, Fagan Paul J., Hauptman Elisabeth, Bullock R. Morris: Metal-Catalyzed Selective Deoxygenation of Diols to Alcohols. Angew Chem 2001, 113, 4005. <http://dx.doi.org/10.1002/1521-3757(20011015)113:20<4005::AID-ANGE4005>3.0.CO;2-9>
• Schlaf Marcel, Ghosh Prasenjit, Fagan Paul J., Hauptman Elisabeth, Bullock R. Morris: Metal-Catalyzed Selective Deoxygenation of Diols to Alcohols. Angew Chem Int Ed 2001, 40, 3887. <http://dx.doi.org/10.1002/1521-3773(20011015)40:20<3887::AID-ANIE3887>3.0.CO;2-Q>
• Müller Christoph, Diehl Volker, Lichtenthaler Frieder W.: Building blocks from sugars. Part 23. Hydrophilic 3-pyridinols from fructose and isomaltulose. Tetrahedron 1998, 54, 10703. <http://dx.doi.org/10.1016/S0040-4020(98)00634-6>