Paper
Chemoenzymatic synthesis of glycosylated enantiomerically pure 4-pentene 1,2- and 1,3-diol derivatives
Published Mar 13, 1998 · F. Bien, T. Ziegler
Tetrahedron-asymmetry
UNKNOWN SJR score
23
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
Chemoenzymatic synthesis of enantiomerically pure 4-pentene 1,2- and 1,3-diol derivatives yields mannopyranosides.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
Sign up to use Study Snapshot
Consensus is limited without an account. Create an account or sign in to get more searches and use the Study Snapshot.
Full text analysis coming soon...
References
Chemoenzymatic synthesis of enantiomerically pure alkene 1,2-diols and glycosides thereof
This study demonstrates the successful kinetic resolution of racemic 2-O-acylated 3-butene-1,2-diol and 1-O-acylated 3-butene-1,2-diol derivatives using various lipases and esterases.
1998·34citations·T. Ziegler et al.·Tetrahedron-asymmetry
Tetrahedron-asymmetry
Small Molecules as Structural and Functional Mimics of Sialyl Lewis X Tetrasaccharide in Selectin Inhibition: A Remarkable Enhancement of Inhibition by Additional Negative Charge and/or Hydrophobic Group
Sialyl Lewis X (SLex) mimics with negative charge or hydrophobic group can effectively inhibit E-, P-, and L-selectins, with IC50 in the low micromolar to high nanomolar range.
1997·81citations·Chi‐Huey Wong et al.·Journal of the American Chemical Society
Journal of the American Chemical Society
A one pot synthesis of ?-(alkoxysilyl)acetic esters
This study developed a one-pot synthesis of?-(alkoxysilyl)acetic esters using Si-H insertion of carbenes, rhodium catalyzed decomposition of diazoacetic esters, and nucleophilic displacement of Cl by ROH.
1993·31citations·Olivier Andrey·Tetrahedron Letters
Tetrahedron Letters
Application of the hydrogenphosphonate approach in the synthesis of glycosyl phosphosugars linked through secondary hydroxyl groups
The hydrogenphosphonate approach effectively synthesizes glycosyl phosphosugars linked through secondary hydroxyl groups, yielding 67-87% of the desired products in the presence of Me3 CCOCl.
1990·34citations·A. Nikolaev et al.·Carbohydrate Research
Carbohydrate Research
π-Cyclizations of α-methoxycarbonyl oxycarbenium ions; synthesis of oxacyclic carboxylic esters
Acid-mediated cyclization reactions of methyl 2-acetoxy-2-(3-alken-1-oxy)acetates lead to the formation of tetrahydropyrans with equatorial carbomethoxy functions and axial chlorine atoms.
1994·29citations·L. D. Lolkema et al.·Tetrahedron
Tetrahedron
Citations
VaporSPOT: Parallel Synthesis of Oligosaccharides on Membranes
VaporSPOT enables simultaneous synthesis of oligosaccharides on cellulose membranes, paving the way for parallel automated glycan synthesis platforms.
2022·5citations·A. Tsouka et al.·Journal of the American Chemical Society
Journal of the American Chemical Society
Candida albicans steryl 6-O-acyl-α-D-mannosides agonize signalling through Mincle.
Candida albicans mycelium produces cholesteryl and ergosteryl 6-O-acyl--d-mannosides, which signal through the human and mouse Mincle receptors, potentially contributing to its pathobiology.
2020·3citations·Tram Nguyen et al.·Chemical communications
Chemical communications
A Photoswitchable Trivalent Cluster Mannoside to Probe the Effects of Ligand Orientation in Bacterial Adhesion
The photoswitchable trivalent cluster mannoside can switch bacterial adhesion to surfaces by reversibly changing its orientation, highlighting the importance of orientational effects in carbohydrate recognition.
2019·6citations·G. Despras et al.·ChemBioChem
ChemBioChem
Synthetic glycoconjugates characterize the fine specificity of Brucella A and M monoclonal antibodies.
Fine specificity of Brucella A and M monoclonal antibodies is based on unique synthetic glycoconjugates, enabling discrimination between closely related A and M epitopes in the O-polysaccharide.
2017·6citations·S. S. Mandal et al.·Organic & biomolecular chemistry
Organic & biomolecular chemistry
Recent advances in the synthesis of fungal antigenic oligosaccharides
This study presents new synthetic blocks, efficient glycoside bond construction, and a novel strategy for preparing furanoside-containing oligosaccharides for fungal antigenic studies.
2016·9citations·V. Krylov et al.·Pure and Applied Chemistry
Pure and Applied Chemistry