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Direct Formation of β-Mannopyranosides and Other Hindered Glycosides from Thioglycosides

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inferred← citeshttps://doi.org/10.2139/ssrn.4659364openalex-extracted
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19981116)110:22<3367::aid-ange3367>3.0.co;2-popenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19990503)111:9<1330::aid-ange1330>3.0.co;2-ropenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19991115)111:22<3535::aid-ange3535>3.0.co;2-sopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/047084289x.rn00419openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/047084289x.rs032.pub3openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/047084289x.rs032.pub4openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/1521-3757(20010302)113:5<972::aid-ange972>3.0.co;2-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/1521-3757(20010504)113:9<1624::aid-ange16240>3.0.co;2-nopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/1521-3773(20010302)40:5<946::aid-anie946>3.0.co;2-gopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470048672.wecb194openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470638859.conrr354openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470842898.rs032.pub3openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780471264194.fos00689openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119006435.ch5openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527618255.ch13openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527618255.ch4openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527618255.ch5openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527621644.ch4aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9783527658947.ch5openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200602642openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200802036openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201100125openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200802036openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201100125openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201408910openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201902507openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202007209openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202111035openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/asia.200900765openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/asia.201801740openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200390009openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.200701864openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201001295openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201402433openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201500648openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chin.199819220openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.201900419openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.200400616openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.200600759openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.200700048openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201001278openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201501464openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.201701579openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ejoc.70599openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/tcr.202100201openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/128_2010_107openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/3-540-30031-7_144openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-03751-6_65-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-03979-4_146openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-16298-0_65openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-540-30429-6_30openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-01053-8_137openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-56874-9_37openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-662-11893-1_13openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-662-46848-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10457-018-0298-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11172-015-1251-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s41061-018-0205-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.11578-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-817592-7.00010-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-819475-1.00016-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-819475-1.00017-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-91099-6.00001-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-91729-2.00014-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00001-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-012312085-4/50006-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.accb.2022.10.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2010.04.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carbpol.2024.122220openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2004.11.025openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2006.09.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2009.07.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2010.02.027openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2013.09.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2013.10.017openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2013.11.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2014.07.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2015.09.009openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2017.10.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2021.108421openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.carres.2025.109396openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cclet.2021.12.065openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ddtec.2020.11.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gresc.2024.03.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2004.04.009openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2004.04.071openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2005.08.090openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2008.03.103openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2010.06.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetasy.2004.10.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.09.132openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.10.158openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.11.160openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.04.017openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.09.064openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.04.060openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.12.077openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154391openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(98)01202-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4020(99)01053-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01329-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01497-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01603-8openalex-snapshot
Synthetic studies on novel fucosylated glycosphingolipids from the millipede, Parafontaria laminata armigera
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)00674-8openalex-snapshot
Novel stereocontrolled α- and β-glycosidations of mannopyranosyl sulfoxides using environmentally benign heterogeneous solid acids
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01133-9openalex-snapshot
Synthesis of arabinofuranosides via low-temperature activation of thioglycosides
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)01402-2openalex-snapshot
Novel and convenient method for the syntheses of 2,6-dideoxypyranoses, 3,6-dideoxypyranoses, and azido (amino) analogs of 3,6-dideoxypyranoses
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)00101-1openalex-snapshot
A concise route to the core pentasaccharide of N-linked glycoproteins
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)00102-3openalex-snapshot
A short synthesis of the trisaccharide building block of the N-linked glycans
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01163-0openalex-snapshot
A practical synthesis of β-d-mannopyranosides
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01837-1openalex-snapshot
First synthesis of anomeric sulfimides - efficient glycosyl donors
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)02159-5openalex-snapshot
Convergent, stereoselective synthesis of the caloporoside disaccharide
inferred← citeshttps://doi.org/10.1016/s0065-2318(04)59003-0openalex-snapshot
SYNTHESIS AND REACTIONS OF GLYCOSIDES
inferred← citeshttps://doi.org/10.1016/s0065-2318(09)00006-7openalex-snapshot
Chapter 6 Stereocontrolled Synthesis of Mannans and Rhamnans
inferred← citeshttps://doi.org/10.1016/s0957-4166(99)00487-5openalex-snapshot
A new glycosylation strategy for the synthesis of mannopyranosides
inferred← citeshttps://doi.org/10.1016/s1874-5296(00)80015-7openalex-snapshot
Iodine, a versatile reagent in carbohydrate chemistry
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00243openalex-snapshot
Mechanisms of Stereodirecting Participation and Ester Migration from Near and Far in Glycosylation and Related Reactions
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00051openalex-snapshot
Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00624openalex-snapshot
Nucleoside Analog Natural Products: Over a Decade of Advances in Isolation, Biological Activity, and Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00402openalex-snapshot
Total Synthesis of Phospholipomannan of Candida albicans
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01834openalex-snapshot
Synthetic Carbohydrate Chemistry and Translational Medicine
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02045openalex-snapshot
Conformationally Constrained Glycosyl Donors as Tools to Control Glycosylation Outcomes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01009openalex-snapshot
Reinvestigation of N,N-Diacetylimido-Protected 2-Aminothioglycosides in O-Glycosylation: Intermolecular Hydrogen Bonds Contributing to 1,2-Orthoamide Formation
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02091openalex-snapshot
Zinc(II) Iodide-Directed β-Mannosylation: Reaction Selectivity, Mode, and Application
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00184openalex-snapshot
One-Pot Glycosylation Strategy Assisted by Ion Mobility–Mass Spectrometry Analysis toward the Synthesis of N-Linked Oligosaccharides
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00725openalex-snapshot
β-Glycosylations with 2-Deoxy-2-(2,4-dinitrobenzenesulfonyl)-amino-glucosyl/galactosyl Selenoglycosides: Assembly of Partially N-Acetylated β-(1 → 6)-Oligoglucosaminosides
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02397openalex-snapshot
Exploring the Dual Functions of Distal Acyl Group Direction in Various Nucleophilic Environments
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02486openalex-snapshot
Zn(NTf 2 ) 2 /NIS as a New Promoter System for Thioglycosides to Effectively Construct α-Galactosamines and α-Galactosazides
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02956openalex-snapshot
The Stereochemical Outcome of Galactosylations Is Influenced by Both the Position and Electron-Withdrawing Power of Distal Acyl Protecting Groups
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00140openalex-snapshot
Construction of β-Mannosidic Bonds via Gold(I)-Catalyzed Glycosylations with Mannopyranosyl ortho-Hexynylbenzoates and Its Application in Synthesis of Acremomannolipin A
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02852openalex-snapshot
Glycosylation of Nucleosides
inferred← citeshttps://doi.org/10.1021/acs.joc.6b03017openalex-snapshot
Deactivating Influence of 3-O-Glycosyl Substituent on Anomeric Reactivity of Thiomannoside Observed in Oligomannoside Synthesis
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00117openalex-snapshot
Mild Activation of 2-Pyridyl 1-Thioglycosides as Stable Donors for α-Stereoselective Glycosylation
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01850openalex-snapshot
Trifluoromethanesulfonate Anion as Nucleophile in Organic Chemistry
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00101openalex-snapshot
Total Synthesis of Tiacumicin A. Total Synthesis, Relay Synthesis, and Degradation Studies of Fidaxomicin (Tiacumicin B, Lipiarmycin A3)
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03056openalex-snapshot
Manual and Automated Syntheses of the N-Linked Glycoprotein Core Glycans
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02405openalex-snapshot
ZnI 2 -Directed Stereocontrolled α-Glucosylation
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02566openalex-snapshot
β- l -Rhamnosylation and β- d -Mannosylation Mediated by 4- O -Ester Groups in a Weakly Nucleophilic Environment
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00295openalex-snapshot
2-Nitro-thioglycosides: α- and β-Selective Generation and Their Potential as β-Selective Glycosyl Donors
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01602openalex-snapshot
Total Synthesis of the Glycosylated Macrolide Antibiotic Fidaxomicin
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00926openalex-snapshot
Glycosyl-Acceptor-Derived Borinic Ester-Promoted Direct and β-Stereoselective Mannosylation with a 1,2-Anhydromannose Donor
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01979openalex-snapshot
Stereodivergent Mannosylation Using 2-O-(ortho-Tosylamido)benzyl Group
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02669openalex-snapshot
Total Synthesis of Trisaccharide Repeating Unit of O-Specific Polysaccharide of Pseudomonas fluorescens BIM B-582
inferred← citeshttps://doi.org/10.1021/acscatal.0c05378openalex-snapshot
Facile Enzymatic Synthesis of Diverse Naturally-Occurring β- d -Mannopyranosides Catalyzed by Glycoside Phosphorylases
inferred← citeshttps://doi.org/10.1021/acsinfecdis.2c00442openalex-snapshot
Large-Scale Synthesis of Man9GlcNAc2 High-Mannose Glycan and the Effect of the Glycan Core on Multivalent Recognition by HIV Antibody 2G12
inferred← citeshttps://doi.org/10.1021/acsinfecdis.7b00008openalex-snapshot
A Natural Lipotrisaccharide and Its Derivatives Selectively Lyse Streptococcus pneumoniae via Interaction with Cell Membrane
inferred← citeshttps://doi.org/10.1021/acsomega.5c03675openalex-snapshot
Synthesis of the Tetrasaccharide Repeating Unit from Klebsiella pneumoniae Serotype K2 Capsular Polysaccharide
inferred← citeshttps://doi.org/10.1021/bk-2012-1102.ch010openalex-snapshot
Systematic Synthesis of Aminosugars and Their Stereoselective Glycosylation
inferred← citeshttps://doi.org/10.1021/bk-2018-1290.ch008openalex-snapshot
Advances in Synthetic Approaches towards Glycoantigens
inferred← citeshttps://doi.org/10.1021/bk-2026-1528.ch003openalex-snapshot
Metal Salts Catalyzed Stereoselective O-Glycosylation with an Armed Glycosyl Trichloroacetimidates Donor
inferred← citeshttps://doi.org/10.1021/cr300436aopenalex-snapshot
Recent Developments in Catalytic Asymmetric Inverse-Electron-Demand Diels–Alder Reaction
inferred← citeshttps://doi.org/10.1021/cr500434xopenalex-snapshot
Mechanisms of Glycosylation Reactions Studied by Low-Temperature Nuclear Magnetic Resonance
inferred← citeshttps://doi.org/10.1021/cs3002513openalex-snapshot
Recent Advances in Transition Metal-Catalyzed Glycosylation
inferred← citeshttps://doi.org/10.1021/ja026186eopenalex-snapshot
Electron Density of Semi-Bridging Carbonyls. Metamorphosis of CO Ligands Observed via Experimental and Theoretical Investigations on [FeCo(CO)8]-
inferred← citeshttps://doi.org/10.1021/ja403609xopenalex-snapshot
Synthesis and Vaccine Evaluation of the Tumor-Associated Carbohydrate Antigen RM2 from Prostate Cancer
inferred← citeshttps://doi.org/10.1021/ja4056678openalex-snapshot
‘Naked’ and Hydrated Conformers of the Conserved Core Pentasaccharide of N-linked Glycoproteins and Its Building Blocks
inferred← citeshttps://doi.org/10.1021/ja405990zopenalex-snapshot
Chemical Synthesis of Highly Congested gp120 V1V2 N-Glycopeptide Antigens for Potential HIV-1-Directed Vaccines
inferred← citeshttps://doi.org/10.1021/ja710935zopenalex-snapshot
Stereoselective Direct Glycosylation with Anomeric Hydroxy Sugars by Activation with Phthalic Anhydride and Trifluoromethanesulfonic Anhydride Involving Glycosyl Phthalate Intermediates
inferred← citeshttps://doi.org/10.1021/ja801574qopenalex-snapshot
Stereoselective Synthesis of β- l -Rhamnopyranosides
inferred← citeshttps://doi.org/10.1021/ja8028137openalex-snapshot
Toward a Prostate Specific Antigen-Based Prostate Cancer Diagnostic Assay: Preparation of Keyhole Limpet Hemocyanin -Conjugated Normal and Transformed Prostate Specific Antigen Fragments
inferred← citeshttps://doi.org/10.1021/ja809554xopenalex-snapshot
Toward Fully Synthetic Homogeneous β-Human Follicle-Stimulating Hormone (β-hFSH) with a Biantennary N-Linked Dodecasaccharide. Synthesis of β-hFSH with Chitobiose Units at the Natural Linkage Sites
inferred← citeshttps://doi.org/10.1021/ja907252uopenalex-snapshot
β-Directing Effect of Electron-Withdrawing Groups at O-3, O-4, and O-6 Positions and α-Directing Effect by Remote Participation of 3-O-Acyl and 6-O-Acetyl Groups of Donors in Mannopyranosylations
inferred← citeshttps://doi.org/10.1021/ja983504uopenalex-snapshot
Synthesis of Vancomycin from the Aglycon
inferred← citeshttps://doi.org/10.1021/ja993004gopenalex-snapshot
Chemoenzymatic Synthesis of α-(1→3)-Gal(NAc)-Terminating Glycosides of Complex Tertiary Sugar Alcohols
inferred← citeshttps://doi.org/10.1021/jacs.0c00447openalex-snapshot
One-Pot Relay Glycosylation
inferred← citeshttps://doi.org/10.1021/jacs.0c03165openalex-snapshot
Fluoride Migration Catalysis Enables Simple, Stereoselective, and Iterative Glycosylation
inferred← citeshttps://doi.org/10.1021/jacs.0c04255openalex-snapshot
Highly Selective β-Mannosylations and β-Rhamnosylations Catalyzed by Bis-thiourea
inferred← citeshttps://doi.org/10.1021/jacs.2c05859openalex-snapshot
The Influence of the Electron Density in Acyl Protecting Groups on the Selectivity of Galactose Formation
inferred← citeshttps://doi.org/10.1021/jacs.2c05953openalex-snapshot
Chemical Synthesis and Antigenicity Evaluation of Shigella dysenteriae Serotype 10 O-Antigen Tetrasaccharide Containing a ( S )-4,6- O -Pyruvyl Ketal
inferred← citeshttps://doi.org/10.1021/jacs.4c03814openalex-snapshot
Chemical Synthesis and Antigenicity Evaluation of an Aminoglycoside Trisaccharide Repeating Unit of Pseudomonas aeruginosa Serotype O5 O-Antigen Containing a Rare Dimeric-Man p N3NA
inferred← citeshttps://doi.org/10.1021/jacs.4c15084openalex-snapshot
Stereoselective Glycosylation for 1,2- cis -Aminoglycoside Assembly by Cooperative Atom Transfer Catalysis
inferred← citeshttps://doi.org/10.1021/jacs.6b08874openalex-snapshot
β-Stereoselective Mannosylation Using 2,6-Lactones
inferred← citeshttps://doi.org/10.1021/jacs.7b07020openalex-snapshot
o -( p -Methoxyphenylethynyl)phenyl Glycosides: Versatile New Glycosylation Donors for the Highly Efficient Construction of Glycosidic Linkages
inferred← citeshttps://doi.org/10.1021/jacs.9b07022openalex-snapshot
Matching Glycosyl Donor Reactivity to Sulfonate Leaving Group Ability Permits SN2 Glycosylations
inferred← citeshttps://doi.org/10.1021/jo010570xopenalex-snapshot
Synthesis of Di- to Hexasaccharide 1,2-Linked β-Mannopyranan Oligomers, a Terminal S-Linked Tetrasaccharide Congener and the Corresponding BSA Glycoconjugates
inferred← citeshttps://doi.org/10.1021/jo0108818openalex-snapshot
Synthesis of the Salmonella Type E1 Core Trisaccharide as a Probe for the Generality of 1-(Benzenesulfinyl)piperidine/Triflic Anhydride Combination for Glycosidic Bond Formation from Thioglycosides
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