Pure and Applied Chemistry

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• Geng Xiaopeng, Cui Bing, Li Yan, Jin Weiping, An Yaping, Zhou Bin, Ye Ting, He Lei, Liang Hongshan, Wang Ling, Chen Yijie, Li Bin: Preparation and characterization of ovalbumin and carboxymethyl cellulose conjugates via glycosylation. Food Hydrocolloids 2014, 37, 86. <http://dx.doi.org/10.1016/j.foodhyd.2013.10.027>
• Kumar Vajinder, Taxak Nikhil, Jangir Ramniwas, Bharatam Prasad V., Kartha K. P. Ravindranathan: In(III) Triflate-Mediated Solvent-Free Synthesis and Activation of Thioglycosides by Ball Milling and Structural Analysis of Long Chain Alkyl Thioglycosides by TEM and Quantum Chemical Methods. J. Org. Chem. 2014, 140408064348001. <http://dx.doi.org/10.1021/jo5001753>
• Temme J. Sebastian, Drzyzga Michael G., MacPherson Iain S., Krauss Isaac J.: Directed Evolution of 2G12-Targeted Nonamannose Glycoclusters by SELMA. Chem. Eur. J. 2013, 19, 17291. <http://dx.doi.org/10.1002/chem.201303848>
• Titov Denis V., Gening Marina L., Gerbst Alexey G., Chizhov Alexander O., Tsvetkov Yury E., Nifantiev Nikolay E.: Stereochemistry of intramolecular cyclization of tetra-β-(1→6)-d-glucosamines and related tetrasaccharides: the role of the conformational stereocontrol and the neighboring group participation. Carbohydrate Research 2013, 381, 161. <http://dx.doi.org/10.1016/j.carres.2012.12.005>
• Ranade Sneha C., Demchenko Alexei V.: Mechanism of Chemical Glycosylation: Focus on the Mode of Activation and Departure of Anomeric Leaving Groups. Journal of Carbohydrate Chemistry 2013, 32, 1. <http://dx.doi.org/10.1080/07328303.2012.749264>
• Nogueira Jason M., Issa John Paul, Chu An-Hsiang Adam, Sisel Jordan A., Schum Ryan S., Bennett Clay S.: Halide Effects on Cyclopropenium Cation Promoted Glycosylation with Deoxy Sugars: Highly α-Selective Glycosylations Using a 3,3-Dibromo-1,2-diphenylcyclopropene Promoter. Eur. J. Org. Chem. 2012, 2012, 4927. <http://dx.doi.org/10.1002/ejoc.201200907>
• Murai Rie, Shirahata Tatsuya, Yamamoto Daisuke, Makino Kazuishi, Kaji Eisuke, Nishino Takashi, Ohya Yohei: Regioselective Glycosylation of Unprotected Methyl Hexopyranoside by Transient Masking with Arylboronic Acid. Heterocycle 2012, 84, 1123. <http://dx.doi.org/10.3987/COM-11-S(P)94>
• Wu Yan-Chao, Li Hui-Jing, Liu Li, Demoulin Nicolas, Liu Zhe, Wang Dong, Chen Yong-Jun: Hafnium Triflate as an Efficient Catalyst for Direct Friedel-Crafts Reactions of Chromene Hemiacetals. Synth Catal 2011, 353, 907. <http://dx.doi.org/10.1002/adsc.201000930>
• SINAY P.: ChemInform Abstract: Recent Advances in Glycosylation Reactions. ChemInform 2010, 22, no. <http://dx.doi.org/10.1002/chin.199139311>
• Shirahata Tatsuya, Matsuo Jun-ichi, Teruya Satoko, Hirata Nozomu, Kurimoto Taku, Akimoto Nanao, Sunazuka Toshiaki, Kaji Eisuke, Ōmura Satoshi: Improved catalytic and stereoselective glycosylation with glycosyl N-trichloroacetylcarbamate: application to various 1-hydroxy sugars. Carbohydrates Research 2010, 345, 740. <http://dx.doi.org/10.1016/j.carres.2010.01.011>
• Kaji Eisuke, Nishino Takashi, Ishige Koji, Ohya Yohei, Shirai Yuko: Regioselective glycosylation of fully unprotected methyl hexopyranosides by means of transient masking of hydroxy groups with arylboronic acids. Tetrahetron Lett 2010, 51, 1570. <http://dx.doi.org/10.1016/j.tetlet.2010.01.048>
• Khaja Sirajud D., Kumar Vipin, Ahmad Misbah, Xue Jun, Matta Khushi L.: Novel galactosyl donor with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position: efficient synthesis of α-galactosyl ceramide. Tetrahetron Lett 2010, 51, 4411. <http://dx.doi.org/10.1016/j.tetlet.2010.06.071>
• Wang Yun, Zhang Xin, Wang Pengfei: Facile glycosylation strategy with two-stage activation of allyl glycosyl donors. Application to concise synthesis of Shigella flexneri serotype Y O-antigen. Org Biomol Chem 2010, 8, 4322. <http://dx.doi.org/10.1039/c002865g>
• Bellomo Ana, Bonilla Julia B., López-Prados Javier, Martín-Lomas Manuel, Gonzalez David: Chemoenzymatic synthesis of glycosyl-deoxyinositol derivatives. First example of a fagopyritol β-analogue containing an aminoinositol unit. Tet Asymm 2009, 20, 2061. <http://dx.doi.org/10.1016/j.tetasy.2009.08.011>
• Stalford Susanne A., Kilner Colin A., Leach Andrew G., Turnbull W. Bruce: Neighbouring group participation vs. addition to oxacarbenium ions: studies on the synthesis of mycobacterial oligosaccharides. Org Biomol Chem 2009, 7, 4842. <http://dx.doi.org/10.1039/b914417j>
• Wang Zerong Daniel, Sheikh Samia O., Cox Shannon, Zhang Yulu, Massey Keegan: Direct Preparation of N-Glycosidic Bond-Linked Nonionic Carbohydrate-Based Surfactant (NICBS) via Ritter Reaction. Eur J Org Chem 2007, 2007, 2243. <http://dx.doi.org/10.1002/ejoc.200700079>
• Kojima Masaru, Nakamura Yutaka, Takeuchi Seiji: A practical fluorous benzylidene acetal protecting group for a quick synthesis of disaccharides. Tetrahetron Lett 2007, 48, 4431. <http://dx.doi.org/10.1016/j.tetlet.2007.04.106>
• Benksim Abdelhafid, Massoui Mohamed, Beaupère Daniel, Wadouachi Anne: Efficient O-glycosylation of diethyl oxoglutarate via 1,2-O-sulfinyl derivatives. Tetrahetron Lett 2007, 48, 5087. <http://dx.doi.org/10.1016/j.tetlet.2007.05.083>
• Sasaki Kaname, Matsumura Shuichi, Toshima Kazunobu: Toward the total synthesis of vineomycin B2: application of an efficient glycosylation methodology using 2,3-unsaturated sugars. Tetrahetron Lett 2007, 48, 6982. <http://dx.doi.org/10.1016/j.tetlet.2007.07.145>
• Galonić Danica P., Gin David Y.: Chemical glycosylation in the synthesis of glycoconjugate antitumour vaccines. Appl Opt 2007, 446, 1000. <http://dx.doi.org/10.1038/nature05813>
• Li Xue-Bing, Ogawa Masato, Monden Toshiki, Maeda Takahiro, Yamashita Eri, Naka Mariko, Matsuda Masao, Hinou Hiroshi, Nishimura Shin-Ichiro: Glycosidation Promoted by a Reusable Solid Superacid in Supercritical Carbon Dioxide. Angew Chem 2006, 118, 5780. <http://dx.doi.org/10.1002/ange.200602161>
• Baek Ju Yuel, Choi Tae Jin, Jeon Heung Bae, Kim Kwan Soo: A Highly Reactive and Stereoselective β-Mannopyranosylation System: Mannosyl 4-Pentenoate/PhSeOTf. Angew Chem 2006, 118, 7596. <http://dx.doi.org/10.1002/ange.200602642>
• Li Xue-Bing, Ogawa Masato, Monden Toshiki, Maeda Takahiro, Yamashita Eri, Naka Mariko, Matsuda Masao, Hinou Hiroshi, Nishimura Shin-Ichiro: Glycosidation Promoted by a Reusable Solid Superacid in Supercritical Carbon Dioxide. Angew Chem Int Ed 2006, 45, 5652. <http://dx.doi.org/10.1002/anie.200602161>
• Baek Ju Yuel, Choi Tae Jin, Jeon Heung Bae, Kim Kwan Soo: A Highly Reactive and Stereoselective β-Mannopyranosylation System: Mannosyl 4-Pentenoate/PhSeOTf. Angew Chem Int Ed 2006, 45, 7436. <http://dx.doi.org/10.1002/anie.200602642>
• Toshima Kazunobu: Novel glycosylation methods and their application to natural products synthesis. Carbohydrates Research 2006, 341, 1282. <http://dx.doi.org/10.1016/j.carres.2006.03.012>
• Matsuo Jun-ichi, Shirahata Tatsuya, Ōmura Satoshi: Catalytic and stereoselective glycosylation with glycosyl N-trichloroacetylcarbamate. Tetrahetron Lett 2006, 47, 267. <http://dx.doi.org/10.1016/j.tetlet.2005.11.027>
• Nishikubo Yuichi, Sasaki Kaname, Matsumura Shuichi, Toshima Kazunobu: One-step syntheses of alkyl glycosides and alkyl-substituted DNA oligomers by chemoselective glycosidations using DNA bases. Tetrahetron Lett 2006, 47, 1041. <http://dx.doi.org/10.1016/j.tetlet.2005.12.049>
• Sasaki Kaname, Matsumura Shuichi, Toshima Kazunobu: An efficient glycosidation method using 2,3-unsaturated glycosyl donors. Tetrahetron Lett 2006, 47, 9039. <http://dx.doi.org/10.1016/j.tetlet.2006.10.095>
• Yang Xiaoliang, Sun Yang, Xu Qiang, Guo Zijian: Synthesis and immunosuppressive activity of l-rhamnopyranosyl flavonoids. Org Biomol Chem 2006, 4, 2483. <http://dx.doi.org/10.1039/b604521a>
• Mandai Hiroki, Mukaiyama Teruaki: 6-Nitro-2-benzothiazolyl α-Mannoside: A Highly Efficient Mannosyl Donor in Constructing β-Man(1→4)GlcN Linkage and Its Application to the Synthesis of the Pentasaccharide Core of N-Glycans. Bull Chem Soc Jpn 2006, 79, 479. <http://dx.doi.org/10.1246/bcsj.79.479>
• Nagai Hideyuki, Sasaki Kaname, Matsumura Shuichi, Toshima Kazunobu: Environmentally benign β-stereoselective glycosidations of glycosyl phosphites using a reusable heterogeneous solid acid, montmorillonite K-10. Carbohydrates Research 2005, 340, 337. <http://dx.doi.org/10.1016/j.carres.2004.11.025>
• Madhusudan Soni Kamlesh, Agnihotri Geetanjali, Negi Devendra S., Misra Anup Kumar: Direct one-pot conversion of acylated carbohydrates into their alkylated derivatives under heterogeneous reaction conditions using solid NaOH and a phase transfer catalyst. Carbohydrates Research 2005, 340, 1373. <http://dx.doi.org/10.1016/j.carres.2005.03.007>
• Pellissier Hélène: Use of O-glycosylation in total synthesis. Tetrahedron 2005, 61, 2947. <http://dx.doi.org/10.1016/j.tet.2005.01.070>
• Sato Ken-ichi, Akai Shoji, Sakai Koudai, Kojima Masaru, Murakami Hideshige, Idoji Tetsuya: Convenient construction of a variety of glycosidic linkages using a universal glucosyl donor. Tetrahetron Lett 2005, 46, 7411. <http://dx.doi.org/10.1016/j.tetlet.2005.08.109>
• Kobashi Yohei, Mukaiyama Teruaki: Glycosyl Phosphonium Halide as a Reactive Intermediate in Highly α-Selective Glycosylation. Bull Chem Soc Jpn 2005, 78, 910. <http://dx.doi.org/10.1246/bcsj.78.910>
• Mukaiyama Teruaki: Strategien zur Erforschung neuer Reaktionen. Angew Chem 2004, 116, 5708. <http://dx.doi.org/10.1002/ange.200300641>
• Mukaiyama Teruaki: Explorations into New Reaction Chemistry. Angew Chem Int Ed 2004, 43, 5590. <http://dx.doi.org/10.1002/anie.200300641>
• Rafiee Ezzat, Tangestaninejad Shahram, Habibi Mohammad H., Mirkhani Valiollah: A mild, efficient and α-selective glycosidation by using potassium dodecatungstocobaltate trihydrate as catalyst. Biorg Med Chem Lett 2004, 14, 3611. <http://dx.doi.org/10.1016/j.bmcl.2004.03.110>
• Toshima Kazunobu, Nagai Hideyuki, Kasumi Ken-ichi, Kawahara Kanako, Matsumura Shuichi: Stereocontrolled glycosidations using a heterogeneous solid acid, sulfated zirconia, for the direct syntheses of α- and β-manno- and 2-deoxyglucopyranosides. Tetrahedron 2004, 60, 5331. <http://dx.doi.org/10.1016/j.tet.2004.04.071>
• Sasaki Kaname, Matsumura Shuichi, Toshima Kazunobu: A novel glycosidation of glycosyl fluoride using a designed ionic liquid and its effect on the stereoselectivity. Tetrahetron Lett 2004, 45, 7043. <http://dx.doi.org/10.1016/j.tetlet.2004.07.128>
• Hashihayata Takashi, Mandai Hiroki, Mukaiyama Teruaki: 6-Nitro-2-benzothiazolyl α-Glucoside and α-Mannoside in β-Selective Glycosylations. Bull Chem Soc Jpn 2004, 77, 169. <http://dx.doi.org/10.1246/bcsj.77.169>
• Nagai Hideyuki, Matsumura Shuichi, Toshima Kazunobu: Environmentally benign and stereoselective formation of β-mannosidic linkages utilizing 2,3-di-O-benzyl-4,6-O-benzylidene-protected mannopyranosyl phosphite and montmorillonite K-10. Carbohydrates Research 2003, 338, 1531. <http://dx.doi.org/10.1016/S0008-6215(03)00234-9>
• Chen Langqiu, Kong Fanzuo: Unusual α-glycosylation with galactosyl donors with a C2 ester capable of neighboring group participation. Tetrahetron Lett 2003, 44, 3691. <http://dx.doi.org/10.1016/S0040-4039(03)00673-7>
• Sasaki Kaname, Nagai Hideyuki, Matsumura Shuichi, Toshima Kazunobu: A novel greener glycosidation using an acid–ionic liquid containing a protic acid. Tetrahetron Lett 2003, 44, 5605. <http://dx.doi.org/10.1016/S0040-4039(03)01376-5>
• Yadav J. S., Reddy B. V. S., Geetha V.: Scandium Triflate Catalyzed Thioglycosidation of Glycals: A Facile Synthesis of 2,3-Unsaturated Thioglycopyranosides. Synth Common 2003, 33, 717. <http://dx.doi.org/10.1081/SCC-120016313>
• Hashihayata Takashi, Ikegai Kazuhiro, Takeuchi Kazuya, Jona Hideki, Mukaiyama Teruaki: Convergent Total Syntheses of Oligosaccharides by One-Pot Sequential Stereoselective Glycosylations. Bull Chem Soc Jpn 2003, 76, 1829. <http://dx.doi.org/10.1246/bcsj.76.1829>
• Abdel-Rahman Adel A.-H., El Ashry El Sayed H., Schmidt Richard R.: Efficient intramolecular β-mannoside formation using m-xylylene and isophthaloyl derivatives as rigid spacers. Carbohydrates Research 2002, 337, 195. <http://dx.doi.org/10.1016/S0008-6215(01)00306-8>
• Nukada Tomoo, Bérces Attila, Whitfield Dennis M.: Can the stereochemical outcome of glycosylation reactions be controlled by the conformational preferences of the glycosyl donor?. Carbohydrates Research 2002, 337, 765. <http://dx.doi.org/10.1016/S0008-6215(02)00043-5>
• Zeng Ying, Ning Jun, Kong Fanzuo: Pure α-linked products can be obtained in high yields in glycosylation with glucosyl trichloroacetimidate donors with a C2 ester capable of neighboring group participation. Tetrahetron Lett 2002, 43, 3729. <http://dx.doi.org/10.1016/S0040-4039(02)00584-1>
• Jona Hideki, Mandai Hiroki, Chavasiri Warinthorn, Takeuchi Kazuya, Mukaiyama Teruaki: Protic Acid Catalyzed Stereoselective Glycosylation Using Glycosyl Fluorides. Bull Chem Soc Jpn 2002, 75, 291. <http://dx.doi.org/10.1246/bcsj.75.291>
• Ejjiyar S., Saluzzo C., Massoui M., Amouroux R., Terry N., Coleman A. W.: Synthesis and assembly properties of a series of chiral amphiphilic dihydroxytetrahydrofuran derivatives. J Phys Org Chem 2001, 14, 1. <http://dx.doi.org/10.1002/1099-1395(200101)14:1<1::AID-POC325>3.0.CO;2-C>
• Nguyen Hien M., Poole Jennifer L., Gin David Y.: Chemoselective Iterative Dehydrative Glycosylation. Angew Chem 2001, 113, 428. <http://dx.doi.org/10.1002/1521-3757(20010119)113:2<428::AID-ANGE428>3.0.CO;2-B>
• Nguyen Hien M., Poole Jennifer L., Gin David Y.: Chemoselective Iterative Dehydrative Glycosylation. Angew Chem Int Ed 2001, 40, 414. <http://dx.doi.org/10.1002/1521-3773(20010119)40:2<414::AID-ANIE414>3.0.CO;2-6>
• Dötz Karl Heinz, Otto Frank, Nieger Martin: Organotransition-metal-modified sugars. J Organomet Chem 2001, 621, 77. <http://dx.doi.org/10.1016/S0022-328X(00)00748-8>
• Kim Ji-Young, Bussolo Valeria Di, Gin David Y.: Stereoselective Synthesis of 2-Hydroxy-α-mannopyranosides from Glucal Donors. Org Lett 2001, 3, 303. <http://dx.doi.org/10.1021/ol006941y>
• Szurmai Zoltán, Rákó János, Ágoston Károly, Danan Alain, Charon Daniel: β-Glycosides of 2,3-Diazido-2,3-dideoxy-d-mannose, a Synthetic Precursor of a Rare Bacterial Cell-Wall Building Unit^†. Org Lett 2000, 2, 1839. <http://dx.doi.org/10.1021/ol0058893>
• Zawisza Anna, Kryczka Boguslaw, Lhoste Paul, Porwanski Stanislaw, Sinou Denis: Efficient Palladium(0)-Catalyzed Synthesis of Alkenyl 1-Thioglycosides and Thiodisaccharides. J Carbohydr Chem 2000, 19, 795. <http://dx.doi.org/10.1080/07328300008544118>
• Jyojima Takaaki, Miyamoto Naoki, Ogawa Yasumasa, Matsumura Shuichi, Toshima Kazunobu: Novel stereocontrolled glycosidations of olivoses using montmorillonite K-10 as an environmentally benign catalyst. Tetrahetron Lett 1999, 40, 5023. <http://dx.doi.org/10.1016/S0040-4039(99)00924-7>
• Babu Boga Sobhana, Balasubramanian Kalpattu Kuppuswamy: Synthesis of 2,3-unsaturated thioglycopyranosides mediated by lithium tetrafluoroborate. Tetrahetron Lett 1999, 40, 5777. <http://dx.doi.org/10.1016/S0040-4039(99)01111-9>
• Pathak Ashish K., Besra Gurdyal S., Crick Dean, Maddry Joseph A., Morehouse Caroline B., Suling William J., Reynolds Robert C.: Studies on β-d-Galf-(1→4)-α-l-Rhap octyl analogues as substrates for mycobacterial galactosyl transferase activity. biorg med chem 1999, 7, 2407. <http://dx.doi.org/10.1016/S0968-0896(99)00199-6>
• von Rybinski Wolfgang, Hill Karlheinz: Alkylpolyglycoside – Eigenschaften und Anwendungen einer neuen Tensidklasse. Angew Chem 1998, 110, 1394. <http://dx.doi.org/10.1002/(SICI)1521-3757(19980518)110:10<1394::AID-ANGE1394>3.0.CO;2-T>
• Frischmuth Katja, Müller Dietrich, Welzel Peter: Strigol synthetic studies the problem of stereocontrol at C-2′. Tetrahedron 1998, 54, 3401. <http://dx.doi.org/10.1016/S0040-4020(98)00075-1>
• Frappa Isabelle, Kryczka Boguslaw, Lhoste Paul, Porwanski Stanislaw, Sinou Denis, Zawisza Anna: Palladium(0)-Mediated Synthesis of Acetylated Unsaturated 1,4-Disaccharides. J Carbohydr Chem 1998, 17, 1117. <http://dx.doi.org/10.1080/07328309808001888>
• Dondoni Alessandro, Marra Alberto, Scherrmann Marie-Christine, Casnati Alessandro, Sansone Francesco, Ungaro Rocco: Synthesis and Properties ofO-Glycosyl Calix[4]Arenes (Calixsugars). Chem Eur J 1997, 3, 1774. <http://dx.doi.org/10.1002/chem.19970031108>
• Zhang Hong, Wang Yali, Thürmer René, Meisenbach Mark, Voelter Wolfgang: Stereoselective Synthesis of the Core Structure of the Nephritogenoside Glycopeptide. Liebigs Ann /Recueil 1997, 1997, 1871. <http://dx.doi.org/10.1002/jlac.199719970910>
• Magaud Didier, Grandjean Cyrille, Doutheau Alain, Anker Daniel, Shevchik Vladimir, Cotte-Pattat Nicole, Robert-Baudouy Janine: An efficient and highly stereoselective α(1→4) glycosylation between two d-galacturonic acid ester derivatives. Tetrahetron Lett 1997, 38, 241. <http://dx.doi.org/10.1016/S0040-4039(96)02308-8>
• Arsequell Gemma, Valencia Gregorio: O-glycosyl α-amino acids as building blocks for glycopeptide synthesis. Tet Asymm 1997, 8, 2839. <http://dx.doi.org/10.1016/S0957-4166(97)00326-1>
• Helmboldt Arnim, Petitou Maurice, Mallet Jean-Maurice, Hérault Jean-Pascal, Lormeau Jean-Claude, Driguez Pierre Alexandre, Herbert Jean-Marc, Sinaÿ Pierre: Synthesis and biological activity of a new anti-factor Xa pentasaccharide with a C-interglycosidic bond. Biorg Med Chem Lett 1997, 7, 1507. <http://dx.doi.org/10.1016/S0960-894X(97)00252-7>
• Zhang Guang-tao, Guo Zhong-wu, Hui Yong-zheng: A Facile Regioselective 1,6-O-Diacetylation Method of Methyl-Glycopyranosides and Their Dimethyl Phosphonates. Synth Common 1997, 27, 1907. <http://dx.doi.org/10.1080/00397919708006792>
• Kimura Teiji, Takayama Shuichi, Huang Hongmei, Wong Chi-Huey: Eine praktikable Synthese vonN-Acetyl-D-lactosamin mit Galactose-Oxidase und β-Galactosidase. Angew Chem 1996, 108, 2503. <http://dx.doi.org/10.1002/ange.19961082010>
• Whitfield D. M., Douglas S. P.: Glycosylation reactions — present status future directions. Glycoconjugate J 1996, 13, 5. <http://dx.doi.org/10.1007/BF01049674>
• Kuwahara Ryuji, Tsuchiya Tsutomu: Synthesis of kanamycin a analogs containing 6-amino-3-oxa-2,3,4,6-tetradeoxy-d- and -l-glycero-hexopyranose. Carbohydrates Research 1996, 286, 107. <http://dx.doi.org/10.1016/0008-6215(96)00051-1>
• Boons Geert-Jan: Strategies in Oligosaccharide Synthesis. Tetrahedron 1996, 52, 1095. <http://dx.doi.org/10.1016/0040-4020(95)00897-7>
• Valverde Serafín, Gómez Ana M., Cristóbal López J., Herradón Bernardo: Template directed cyclo-glycosylation: Effect of the anchoring sites of the spacer and temperature in the regio- and stereo-selectivity of the glycosylation. Tetrahetron Lett 1996, 37, 1105. <http://dx.doi.org/10.1016/0040-4039(95)02316-X>
• Bogusiak Jadwiga, Szeja Wieslaw: Synthesis of glycofuranosides from S-glycofuranosyl dithiocarbonates (xanthates) and dithiocarbamates. Carbohydrates Research 1996, 295, 235. <http://dx.doi.org/10.1016/S0008-6215(96)90148-2>
• Fernandez José Manuel García, Mellet Carmen Ortiz: The Thiocarbonyl Group in Carbohydrate Chemistry. Sulfur Reports 1996, 19, 61. <http://dx.doi.org/10.1080/01961779608047905>
• Li Zhong-Jun, Huang He-Qing, Cai Meng-Shen: Studies on Glycosides XVI. The Use of Mannosyl Trichloroacetate in the Synthesis of α-Mannosides and Related Oligosaccharides. J Carbohydr Chem 1996, 15, 501. <http://dx.doi.org/10.1080/07328309608005669>
• Uchiro Hiromi, Mukaiyama Teruaki: Trityl Salt Catalyzed Stereoselective Glycosylation of Alcohols with 1-Hydroxyribofuranose. Chem Lett 1996, 79. <http://dx.doi.org/10.1246/cl.1996.79>
• Lau Richard, Schüle Gunter, Schwaneberg Ulrich, Ziegler Thomas: Prearranged glycosides, 2. Intramolecular glycosylation of prearranged saccharides as a novel strategy for the construction of β-L-rhamnosidic linkages. Liebigs Ann /Recueil 1995, 1995, 1745. <http://dx.doi.org/10.1002/jlac.1995199510245>
• Li Pan, Sun Lihong, Landry Donald W., Zhao Kang: Synthesis of 1-thioglycosides. Carbohydrates Research 1995, 275, 179. <http://dx.doi.org/10.1016/0008-6215(95)00021-K>
• Perrin Charles L.: Reverse anomeric effect: fact or fiction?. Tetrahedron 1995, 51, 11901. <http://dx.doi.org/10.1016/0040-4020(95)00560-U>
• Sinou Denis, Frappa Isabelle, Lhoste Paul, Porwanski Stanislaw, Kryczka Boguslaw: Stereoselective palladium(0)-mediated synthesis of 1,4-disaccharides. Tetrahetron Lett 1995, 36, 1251. <http://dx.doi.org/10.1016/0040-4039(94)02480-Y>
• Zhang Hong, Wang Yali, Voelter Wolfgang: A new strategy for the synthesis of the nephritogenoside trisaccharide unit using phenylsulfenyl donors. Tetrahetron Lett 1995, 36, 1243. <http://dx.doi.org/10.1016/0040-4039(94)02486-U>
• Hashimoto Shun-ichi, Umeo Kazuhiro, Sano Ai, Watanabe Nobuhide, Nakajima Makoto, Ikegami Shiro: An extremely mild and stereocontrolled construction of 1,2-trans-β-glycosidic linkages capitalizing on benzyl-protected glycopyranosyl diethyl phosphites as glycosyl donors. Tetrahetron Lett 1995, 36, 2251. <http://dx.doi.org/10.1016/0040-4039(95)00263-C>
• Ferrières Vincent, Bertho Jean-Noël, Plusquellec Daniel: A new synthesis of O-glycosides from totally O-unprotected glycosyl donors. Tetrahetron Lett 1995, 36, 2749. <http://dx.doi.org/10.1016/0040-4039(95)00356-H>
• Wang Hui, Sun Lihong, Glazebnik Serge, Zhao Kang: Peralkylation of saccharides under aqueous conditions. Tetrahetron Lett 1995, 36, 2953. <http://dx.doi.org/10.1016/0040-4039(95)00446-J>
• Fuentes José, González-Eulate Enrique, López-Barba Eugenia, Robina Inmaculada: Regioselective Glycosylation of N-Protected l-Rhamno(fuco) pyranosylamines: Preparation and Spectroscopic Characterization of Building Blocks for Neoglycoconjugate Syntheses. J Carbohydr Chem 1995, 14, 79. <http://dx.doi.org/10.1080/07328309508006438>
• Westman Jacob, Nilsson Marianne, Ornitz David M., Svahn Carl-Magnus: Synthesis and Fibroblast Growth Factor Binding of Oligosaccharides Related to Heparin and Heparan Sulphate. J Carbohydr Chem 1995, 14, 95. <http://dx.doi.org/10.1080/07328309508006439>
• Marra Alberto, Scherrmann Marie-Christine, Dondoni Alessandro, Casnati Alessandro, Minari Patrizia, Ungaro Rocco: Zuckercalixarene: Synthese von Calix[4]arenen mitO-Glycosylsubstituenten am oberen oder unteren Rand. Angew Chem 1994, 106, 2533. <http://dx.doi.org/10.1002/ange.19941062317>
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