Статті в журналах з теми "Allyl glycosides"
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Pal, Rita, Anupama Das, and Narayanaswamy Jayaraman. "One-pot oligosaccharide synthesis: latent-active method of glycosylations and radical halogenation activation of allyl glycosides." Pure and Applied Chemistry 91, no. 9 (September 25, 2019): 1451–70. http://dx.doi.org/10.1515/pac-2019-0306.
Повний текст джерелаGibson, Robin R., Roger P. Dickinson, and Geert-Jan Boons. "Vinyl glycosides in oligosaccharide synthesis (part 4): glycosidase-catalysed preparation of substituted allyl glycosides." Journal of the Chemical Society, Perkin Transactions 1, no. 22 (1997): 3357–60. http://dx.doi.org/10.1039/a704703g.
Повний текст джерелаKrähmer, Ralf, Lothar Hennig, Matthias Findeisen, Dietrich Müller, and Peter Welzel. "Oxidative deprotection of allyl glycosides." Tetrahedron 54, no. 36 (September 1998): 10753–60. http://dx.doi.org/10.1016/s0040-4020(98)00640-1.
Повний текст джерелаSherman, Andrei A., Leonid O. Kononov, Alexander S. Shashkov, Georgij V. Zatonsky, and Nikolay E. Nifant’ev. "Synthesis of spacer-armed glycosides using azidophenylselenylation of allyl glycosides." Mendeleev Communications 8, no. 1 (January 1998): 9–11. http://dx.doi.org/10.1070/mc1998v008n01abeh000887.
Повний текст джерелаWang, Pengfei, Pranab Haldar, Yun Wang, and Huayou Hu. "Simple Glycosylation Reaction of Allyl Glycosides." Journal of Organic Chemistry 72, no. 15 (July 2007): 5870–73. http://dx.doi.org/10.1021/jo070512x.
Повний текст джерелаTimmer, Mattie S. M., Marta Vinciano Chumillas, Wilma E. Donker‐Koopman, Johannes M. F. G. Aerts, Gijsbert A. van derMarel, Herman S. Overkleeft, and Jacques H. van Boom. "Selective Cross‐Metathesis ofC‐Allyl‐Glycosides." Journal of Carbohydrate Chemistry 24, no. 4-6 (August 2005): 335–51. http://dx.doi.org/10.1080/07328300500174887.
Повний текст джерелаGIBSON, R. R., R. P. DICKINSON, and G. J. BOONS. "ChemInform Abstract: Vinyl Glycosides in Oligosaccharide Synthesis. Part 4. Glycosidase-Catalyzed Preparation of Substituted Allyl Glycosides." ChemInform 29, no. 14 (June 23, 2010): no. http://dx.doi.org/10.1002/chin.199814171.
Повний текст джерелаHu, Yun-Jin, Romyr Dominique, Sanjoy Kumar Das, and René Roy. "A facile new procedure for the deprotection of allyl ethers under mild conditions." Canadian Journal of Chemistry 78, no. 6 (June 1, 2000): 838–45. http://dx.doi.org/10.1139/v00-073.
Повний текст джерелаKRAEHMER, R., L. HENNIG, M. FINDEISEN, D. MUELLER, and P. WELZEL. "ChemInform Abstract: Oxidative Deprotection of Allyl Glycosides." ChemInform 29, no. 50 (June 18, 2010): no. http://dx.doi.org/10.1002/chin.199850242.
Повний текст джерелаSHERMAN, A. A., L. O. KONONOV, A. S. SHASHKOV, G. V. ZATONSKY, and N. E. NIFANT'EV. "ChemInform Abstract: Synthesis of Spacer-Armed Glycosides Using Azidophenylselenylation of Allyl Glycosides." ChemInform 29, no. 30 (June 20, 2010): no. http://dx.doi.org/10.1002/chin.199830240.
Повний текст джерелаPal, Rita, Anupama Das, and Narayanaswamy Jayaraman. "Radical halogenation-mediated latent–active glycosylations of allyl glycosides." Chemical Communications 54, no. 6 (2018): 588–90. http://dx.doi.org/10.1039/c7cc07332a.
Повний текст джерелаMcGarvey, Glenn J., Christopher A. LeClair, and Bahar A. Schmidtmann. "Studies on the Stereoselective Synthesis ofC-Allyl Glycosides." Organic Letters 10, no. 21 (November 6, 2008): 4727–30. http://dx.doi.org/10.1021/ol801710s.
Повний текст джерелаBellucci, Giuseppe, Cinzia Chiappe, and Felicia D'Andrea. "Diastereoselective bromination of allyl glycosides using tetrabutylammonium tribromide." Tetrahedron: Asymmetry 6, no. 1 (January 1995): 221–30. http://dx.doi.org/10.1016/0957-4166(94)00378-o.
Повний текст джерелаDas, Anupama, and Narayanaswamy Jayaraman. "Carbon tetrachloride-free allylic halogenation-mediated glycosylations of allyl glycosides." Organic & Biomolecular Chemistry 19, no. 42 (2021): 9318–25. http://dx.doi.org/10.1039/d1ob01298c.
Повний текст джерелаJiang, Nan, Zhengliang Wu, Youxian Dong, Xiaoxia Xu, Xiaxia Liu, and Jianbo Zhang. "Progress in the Synthesis of 2,3-unsaturated Glycosides." Current Organic Chemistry 24, no. 2 (April 15, 2020): 184–99. http://dx.doi.org/10.2174/1385272824666200130111142.
Повний текст джерелаLüning, Joachim, Uwe Möller, Norbert Debski, and Peter Welzel. "A new method for the cleavage of allyl glycosides." Tetrahedron Letters 34, no. 37 (September 1993): 5871–74. http://dx.doi.org/10.1016/s0040-4039(00)73801-9.
Повний текст джерелаBai, Yaguang, Wei Lin Leng, Yongxin Li, and Xue-Wei Liu. "A highly efficient dual catalysis approach for C-glycosylation: addition of (o-azaaryl)carboxaldehyde to glycals." Chem. Commun. 50, no. 87 (2014): 13391–93. http://dx.doi.org/10.1039/c4cc06111j.
Повний текст джерелаvan Seeventer, Paul B., Johannes A. L. M. van Dorst, John F. Siemerink, Johannis P. Kamerling, and Johannes F. G. Vliegenthart. "Thiol addition to protected allyl glycosides: An improved method for the preparation of spacer-arm glycosides." Carbohydrate Research 300, no. 4 (May 1997): 369–73. http://dx.doi.org/10.1016/s0008-6215(97)00074-8.
Повний текст джерелаBoons, Geert-Jan, and Stephen Isles. "Vinyl Glycosides in Oligosaccharide Synthesis. 2. The Use of Allyl and Vinyl Glycosides in Oligosaccharide Synthesis." Journal of Organic Chemistry 61, no. 13 (January 1996): 4262–71. http://dx.doi.org/10.1021/jo960131b.
Повний текст джерелаPanchadhayee, Rajib, and Anup Kumar Misra. "N-Bromosuccinimide-Mediated Conversion of Allyl Glycosides to Glycosyl Hemiacetals." Journal of Carbohydrate Chemistry 29, no. 2 (March 22, 2010): 76–83. http://dx.doi.org/10.1080/07328301003664887.
Повний текст джерелаXie, Juan, and Jean-Marc Valéry. "INVESTIGATION OF THE SHARPLESS ASYMMETRIC AMINOHYDROXYLATION WITH C-ALLYL GLYCOSIDES." Journal of Carbohydrate Chemistry 20, no. 6 (July 31, 2001): 441–45. http://dx.doi.org/10.1081/car-100106927.
Повний текст джерелаBELLUCCI, G., C. CHIAPPE, and F. D'ANDREA. "ChemInform Abstract: Diastereoselective Bromination of Allyl Glycosides Using Tetrabutylammonium Tribromide." ChemInform 26, no. 27 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199527050.
Повний текст джерелаKánya, Nándor, Sándor Kun, and László Somsák. "Glycopyranosylidene-Spiro-Morpholinones: Evaluation of the Synthetic Possibilities Based on Glyculosonamide Derivatives and a New Method for the Construction of the Morpholine Ring." Molecules 27, no. 22 (November 11, 2022): 7785. http://dx.doi.org/10.3390/molecules27227785.
Повний текст джерелаSommer, Roman, Dirk Hauck, Annabelle Varrot, Anne Imberty, Markus Künzler, and Alexander Titz. "O-Alkylated heavy atom carbohydrate probes for protein X-ray crystallography: Studies towards the synthesis of methyl 2-O-methyl-L-selenofucopyranoside." Beilstein Journal of Organic Chemistry 12 (December 22, 2016): 2828–33. http://dx.doi.org/10.3762/bjoc.12.282.
Повний текст джерелаKumar, Brijesh, Mushtaq A. Aga, Abdul Rouf, Bhahwal A. Shah та Subhash C. Taneja. "2,3-Unsaturated Allyl Glycosides as Glycosyl Donors for Selective α-Glycosylation". Journal of Organic Chemistry 76, № 9 (6 травня 2011): 3506–10. http://dx.doi.org/10.1021/jo102333x.
Повний текст джерелаKhamsi, Jamal, Roger A. Ashmus, Nathaniel S. Schocker, and Katja Michael. "A high-yielding synthesis of allyl glycosides from peracetylated glycosyl donors." Carbohydrate Research 357 (August 2012): 147–50. http://dx.doi.org/10.1016/j.carres.2012.05.008.
Повний текст джерелаLUENING, J., U. MOELLER, N. DEBSKI, and P. WELZEL. "ChemInform Abstract: A New Method for the Cleavage of Allyl Glycosides." ChemInform 25, no. 4 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199404250.
Повний текст джерелаLopez, J. Cristobal, Fernando Lobo, Silvia Miranda, Clara Uriel, and Ana M. Gomez. "Ferrier–Nicholas pyranosidic cations: application to diversity-oriented synthesis." Pure and Applied Chemistry 86, no. 9 (September 19, 2014): 1357–64. http://dx.doi.org/10.1515/pac-2014-0402.
Повний текст джерелаBOONS, G. J., and S. ISLES. "ChemInform Abstract: Vinyl Glycosides in Oligosaccharide Synthesis. Part 2. The Use of Allyl and Vinyl Glycosides in Oligosaccharide Synthesis." ChemInform 27, no. 45 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199645246.
Повний текст джерелаHu, Yun-Jin, and Rene´ Roy. "Cross-metathesis of N-alkenyl peptoids with O- or C-allyl glycosides." Tetrahedron Letters 40, no. 17 (April 1999): 3305–8. http://dx.doi.org/10.1016/s0040-4039(99)00481-5.
Повний текст джерелаPatnam, Ramesh, Juan M. Juárez-Ruiz, and René Roy. "Subtle Stereochemical and Electronic Effects in Iridium-Catalyzed Isomerization ofC-Allyl Glycosides." Organic Letters 8, no. 13 (June 2006): 2691–94. http://dx.doi.org/10.1021/ol060671n.
Повний текст джерелаXie, Juan, and Jean-Marc Valery. "ChemInform Abstract: Investigation of the Sharpless Asymmetric Aminohydroxylation with C-Allyl Glycosides." ChemInform 33, no. 9 (May 22, 2010): no. http://dx.doi.org/10.1002/chin.200209199.
Повний текст джерелаPanchadhayee, Rajib, and Anup Kumar Misra. "ChemInform Abstract: N-Bromosuccinimide-Mediated Conversion of Allyl Glycosides to Glycosyl Hemiacetals." ChemInform 41, no. 47 (October 28, 2010): no. http://dx.doi.org/10.1002/chin.201047191.
Повний текст джерелаHusein, Husein A., Dhurgham A. H. Alhasan, and Majid A. Z. Albadry. "In Vitro Antimicrobial Activity of Aqueous-Methanolic Extract of Populus sp. Leaves." Basrah Journal of Agricultural Sciences 31, no. 2 (February 8, 2019): 53–64. http://dx.doi.org/10.37077/25200860.2018.102.
Повний текст джерелаKumar, Brijesh, Mushtaq A. Aga, Abdul Rouf, Bhahwal A. Shah та Subhash C. Taneja. "ChemInform Abstract: 2,3-Unsaturated Allyl Glycosides as Glycosyl Donors for Selective α-Glycosylation." ChemInform 42, № 32 (14 липня 2011): no. http://dx.doi.org/10.1002/chin.201132190.
Повний текст джерелаFinch, Paul, George M. Iskander, and Aloysius H. Siriwardena. "Convenient syntheses of 2,3,5-tri-O-benzyl-arabino- and −ribofuranoses via their allyl glycosides." Carbohydrate Research 210 (March 1991): 319–25. http://dx.doi.org/10.1016/0008-6215(91)80132-7.
Повний текст джерелаAspinall, Gerald O., Alexander M. Crane, David W. Gammon, Ibrahim H. Ibrahim, Naveen K. Khare, Delphi Chatterjee, Becky Rivoire, and Patrick J. Brennan. "Synthesis of allyl glycosides for conversion into neoglycoproteins bearing epitopes of mycobacterial glycolipid antigens." Carbohydrate Research 216 (September 1992): 337–55. http://dx.doi.org/10.1016/0008-6215(92)84172-o.
Повний текст джерелаCardona, Francisco, and Barbara La Ferla. "Synthesis of C-Glycoconjugates from Readily Available Unprotected C-Allyl Glycosides by Chemoselective Ligation." Journal of Carbohydrate Chemistry 27, no. 4 (May 2008): 203–13. http://dx.doi.org/10.1080/07328300802082457.
Повний текст джерелаAraki, Younosuke, Naoki Kobayashi, Kazuko Watanabe, and Yoshiharu Ishido. "Synthesis of Glycosyl Cyanides andC-Allyl Glycosides by the use of Glycosyl Fluoride Derivatives." Journal of Carbohydrate Chemistry 4, no. 4 (December 1985): 565–85. http://dx.doi.org/10.1080/07328308508082677.
Повний текст джерелаHu, Yun-Jin, and Rene Roy. "ChemInform Abstract: Cross-Methathesis of N-Alkenyl Peptoids with O- or C-Allyl Glycosides." ChemInform 30, no. 30 (June 14, 2010): no. http://dx.doi.org/10.1002/chin.199930201.
Повний текст джерелаWu, An-Tai, Tian Yi, Huawu Shao, Shih-Hsiung Wu, and Wei Zou. "Stereoselective synthesis of dioxabicycles from 1-C-allyl-2-O-benzyl-glycosides An intramolecular cyclization between 2-O-benzyl oxygen and the allyl double bond." Canadian Journal of Chemistry 84, no. 4 (April 1, 2006): 597–602. http://dx.doi.org/10.1139/v06-046.
Повний текст джерелаKunz, Horst, Herbert Waldmann, and Uwe Klinkhammer. "The Allyl Ester as Carboxy-Protecting Group in the Stereoselective Construction of Neuraminic-Acid Glycosides." Helvetica Chimica Acta 71, no. 8 (December 14, 1988): 1868–74. http://dx.doi.org/10.1002/hlca.19880710804.
Повний текст джерелаButler, Samuel J., Simon Birgersson, Mathias Wiemann, Monica Arcos-Hernandez та Henrik Stålbrand. "Transglycosylation by β-mannanase TrMan5A variants and enzyme synergy for synthesis of allyl glycosides from galactomannan". Process Biochemistry 112 (січень 2022): 154–66. http://dx.doi.org/10.1016/j.procbio.2021.11.028.
Повний текст джерелаAuzanneau, France-Isabelle, Farzin Forooghian, and B. Mario Pinto. "Efficient, convergent syntheses of oligosaccharide allyl glycosides corresponding to the Streptococcus Group A cell-wall polysaccharide." Carbohydrate Research 291 (September 1996): 21–41. http://dx.doi.org/10.1016/s0008-6215(96)00152-8.
Повний текст джерелаAuzanneau, F. "Efficient, convergent syntheses of oligosaccharide allyl glycosides corresponding to the Streptococcus Group A cell-wall polysaccharide." Carbohydrate Research 291, no. 1 (September 23, 1996): 21–41. http://dx.doi.org/10.1016/0008-6215(96)00152-8.
Повний текст джерелаFINCH, P., G. M. ISKANDER, and A. H. SIRIWARDENA. "ChemInform Abstract: Convenient Syntheses of 2,3,5-Tri-O-benzyl-arabino- and -ribofuranoses via Their Allyl Glycosides." ChemInform 23, no. 7 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199207257.
Повний текст джерелаKononov, Leonid O., Göran Magnusson, Marina I. Ferrero, Cesare Rol, Giovanni V. Sebastiani, George W. Francis, József Szúnyog, and Bengt Långström. "Synthesis of Methyl and Allyl alpha-Glycosides of N-Acetylneuraminic Acid in the Absence of Added Promoter." Acta Chemica Scandinavica 52 (1998): 141–44. http://dx.doi.org/10.3891/acta.chem.scand.52-0141.
Повний текст джерелаDi Bussolo, Valeria, Annalisa Fiasella, Maria Rosaria Romano, Lucilla Favero, Mauro Pineschi, and Paolo Crotti. "Stereoselective Synthesis of 2,3-Unsaturated-aza-O-glycosides via New DiastereoisomericN-Cbz-imino Glycal-Derived Allyl Epoxides†." Organic Letters 9, no. 22 (October 2007): 4479–82. http://dx.doi.org/10.1021/ol701836a.
Повний текст джерелаEichler, Eva, Jan Kihlberg, and David R. Bundle. "Access to fluorescent probes via allyl glycosides: the synthesis of aBrucella trisaccharide epitope linked to a coumarin." Glycoconjugate Journal 8, no. 2 (April 1991): 69–74. http://dx.doi.org/10.1007/bf00731014.
Повний текст джерелаPastore, Antonello, Matteo Adinolfi, and Alfonso Iadonisi. "BiBr3-Promoted Activation of Peracetylated Glycosyl Iodides: Straightforward Access to Synthetically Useful 2-O-Deprotected Allyl Glycosides." European Journal of Organic Chemistry 2008, no. 36 (December 2008): 6206–12. http://dx.doi.org/10.1002/ejoc.200800914.
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