Page last updated: 2024-08-25

oxazolidin-2-one and glucosamine

oxazolidin-2-one has been researched along with glucosamine in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (55.56)29.6817
2010's4 (44.44)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Benakli, K; Kerns, RJ; Zha, C1
Crich, D; Vinod, AU1
Kerns, RJ; Wei, P1
Geng, Y; Ye, XS; Zhang, LH1
Eriksson, L; Lahmann, M; Olsson, JD; Oscarson, S1
Carvalho, LC; Dias Pires, MJ; Enugala, R; Marques, MM1
Murakami, T1
Block, TM; Chang, J; Cuconati, A; Du, Y; Gill, T; Guo, F; Guo, JT; Khan, N; Wang, L; Xu, X; Ye, H1
Qin, Q; Xiong, DC; Ye, XS1

Reviews

1 review(s) available for oxazolidin-2-one and glucosamine

ArticleYear
Stereoselective glycosylation of glucosamine: the role of the N-protecting group.
    Chemistry, an Asian journal, 2012, Volume: 7, Issue:11

    Topics: Azides; Biocompatible Materials; Glucosamine; Glycosylation; Oxazolidinones; Polymers; Stereoisomerism

2012

Other Studies

8 other study(ies) available for oxazolidin-2-one and glucosamine

ArticleYear
Oxazolidinone protected 2-amino-2-deoxy-D-glucose derivatives as versatile intermediates in stereoselective oligosaccharide synthesis and the formation of alpha-linked glycosides.
    Journal of the American Chemical Society, 2001, Sep-26, Volume: 123, Issue:38

    Topics: Carbohydrate Conformation; Glucosamine; Glycosaminoglycans; Glycosides; Oligosaccharides; Oxazolidinones; Stereoisomerism

2001
6-O-Benzyl- and 6-O-silyl-N-acetyl-2-amino-2-N,3-O-carbonyl-2-deoxyglucosides: effective glycosyl acceptors in the glucosamine 4-OH Series. effect of anomeric stereochemistry on the removal of the oxazolidinone group.
    The Journal of organic chemistry, 2005, Feb-18, Volume: 70, Issue:4

    Topics: Acetylation; Amination; Deoxyglucose; Glucosamine; Glycosides; Hydroxides; Magnetic Resonance Spectroscopy; Methylation; Molecular Structure; Oxazolidinones; Stereoisomerism; Sulfhydryl Compounds

2005
Factors affecting stereocontrol during glycosidation of 2,3-oxazolidinone-protected 1-tolylthio-N-acetyl-D-glucosamine.
    The Journal of organic chemistry, 2005, May-13, Volume: 70, Issue:10

    Topics: Glucosamine; Glycoconjugates; Glycosides; Glycosylation; Oxazolidinones; Stereoisomerism

2005
Pre-activation protocol leading to highly stereoselectivity-controllable glycosylations of oxazolidinone protected glucosamines.
    Chemical communications (Cambridge, England), 2008, Feb-07, Issue:5

    Topics: Carbohydrate Conformation; Glucosamine; Glycosylation; Oxazolidinones; Stereoisomerism

2008
Investigations of glycosylation reactions with 2-N-acetyl-2N,3O-oxazolidinone-protected glucosamine donors.
    The Journal of organic chemistry, 2008, Sep-19, Volume: 73, Issue:18

    Topics: Carbohydrate Conformation; Crystallography, X-Ray; Disaccharides; Glucosamine; Glycosylation; Mesylates; Models, Molecular; Molecular Structure; Oxazolidinones; Time Factors

2008
Synthesis of all four stereoisomers of 5-formyl-4-hydroxymethyl-1,3-oxazolidin-2-ones from D-glucosamine.
    Carbohydrate research, 2013, Jun-28, Volume: 375

    Topics: Glucosamine; Molecular Structure; Oxazolidinones; Stereoisomerism

2013
Design and synthesis of N-alkyldeoxynojirimycin derivatives with improved metabolic stability as inhibitors of BVDV and Tacaribe virus.
    Bioorganic & medicinal chemistry letters, 2013, Jul-15, Volume: 23, Issue:14

    Topics: 1-Deoxynojirimycin; Animals; Antiviral Agents; Arenaviruses, New World; Diarrhea Viruses, Bovine Viral; Drug Design; Glucosamine; Humans; Mice; Microsomes, Liver; Oxazolidinones; Rats; Sulfonamides; Urea; Virus Replication

2013
Additive-controlled stereoselective glycosylations of 2,3-oxazolidinone protected glucosamine or galactosamine thioglycoside donors with phenols based on preactivation protocol.
    Carbohydrate research, 2015, Feb-11, Volume: 403

    Topics: Galactosamine; Glucosamine; Glycosylation; Oxazolidinones; Phenols; Stereoisomerism; Substrate Specificity; Thioglycosides

2015