about
Carbohydrates as enantioinduction components in stereoselective catalysisGlycosyltransferase activity can be modulated by small conformational changes of acceptor substrates.Substrate specificity of strictosidine synthase.Direct Evidence of Lack of Colocalisation of Fluorescently Labelled Gold Labels Used in Correlative Light Electron Microscopy.Ionic liquids in oligosaccharide synthesis: towards mucin-type glycan probes.Carbohydrate chemistry in drug discovery.Multivalent glyco(cyclo)peptides.Recent developments of ionic liquids in oligosaccharide synthesis: the sweet side of ionic liquids.Imidazolium-tagged glycan probes for non-covalent labeling of live cells.Lactose as a "Trojan horse" for quantum dot cell transport.Substrate specificity and diastereoselectivity of strictosidine glucosidase, a key enzyme in monoterpene indole alkaloid biosynthesis.Platform Synthetic Lectins for Divalent Carbohydrate Recognition in WaterDivalent Naphthalene Diimide Ligands Display High Selectivity for the Human Telomeric G-quadruplex in K+ Buffer.Palladium-Catalyzed Direct Stereoselective Synthesis of Deoxyglycosides from GlycalsPalladium-Catalyzed α-Stereoselective O-Glycosylation of O(3)-Acylated Glycals.A 3,4-trans-fused cyclic protecting group facilitates α-selective catalytic synthesis of 2-deoxyglycosides.Stereoselective Glycosylation of 2-Nitrogalactals Catalyzed by a Bifunctional Organocatalyst.Cooperative Brønsted Acid-Type Organocatalysis for the Stereoselective Synthesis of Deoxyglycosides.Stereoselective synthesis of protected l- and d-dideoxysugars and analogues via Prins cyclisations.Synthesis of mucin-type O-glycan probes as aminopropyl glycosides.Correction: Fluorescent carbon dots from mono- and polysaccharides: synthesis, properties and applications.Scope and limitations of imidazolium-based ionic liquids as room temperature glycosylation promoters.Chemo-enzymatic synthesis of conformationally constrained oligosaccharides.Combinatorial ionic catch-and-release oligosaccharide synthesis (combi-ICROS).Initial stages in the formation of Cu2ZnSn(S,Se)4 nanoparticles.Ionic-liquid-based MS probes for the chemo-enzymatic synthesis of oligosaccharides.Ultraviolet Absorption Induces Hydrogen-Atom Transfer in G⋅C Watson-Crick DNA Base Pairs in Solution.Imidazolium-labeled glycosides as probes to harness glycosyltransferase activity in human breast milk.The design and synthesis of a selective inhibitor of fucosyltransferase VI.Three-minute synthesis of sp(3) nanocrystalline carbon dots as non-toxic fluorescent platforms for intracellular delivery.Is UV-Induced Electron-Driven Proton Transfer Active in a Chemically Modified A·T DNA Base Pair?Gold(I)-Catalyzed Direct Stereoselective Synthesis of Deoxyglycosides from Glycals.Chemo-enzymatic synthesis of imidazolium-tagged sialyllactosamine probes.Redesign of a central enzyme in alkaloid biosynthesis.Glycosyltransferase activity can be selectively modulated by chemical modifications of acceptor substratesα-(2,6)-Sialyltransferase-Catalyzed Sialylations of Conformationally Constrained OligosaccharidesRapid phosphine-free synthesis of CdSe quantum dots: promoting the generation of Se precursors using a radical initiatorQuantum Dot-Based Probes for Labeling and Imaging of Cells that Express Matrix MetalloproteinasesPractical Three-Minute Synthesis of Acid-Coated Fluorescent Carbon Dots with Tuneable Core StructureA Photoresponsive Stiff-Stilbene Ligand Fuels the Reversible Unfolding of G-Quadruplex DNA.
P50
Q28072011-1F45BEA5-F05D-4052-A658-BFCA1ACAFBE5Q30333179-4CC378A9-AB2B-49FC-8CF3-894491C70C41Q34494915-00F8CD5E-6A19-47B2-AF9D-EDFE60E5D652Q36314297-AE42E2CB-F145-4B92-A93A-9ED180A661E7Q37791595-2E6BA088-1685-4FCA-9D83-2BD552440877Q37853437-FFE0ED1D-AC58-454C-8F23-1359E7201241Q38069441-A450C31B-2021-4258-96F9-F58ECDF5153EQ38107729-658FC5D1-996E-428C-879B-9176785F80D5Q38786617-EC479029-B03A-4031-84CC-C01D072B16E8Q39047702-F5A8D4CD-9216-4270-B914-411180A803DCQ40607772-BE1A110A-7329-43B9-85B2-DDE644392E7DQ40987253-C946C56D-E7D5-43B7-BEE8-1F474071C6C4Q41040138-C8347308-3E27-46E2-93EA-4080B90F7B5EQ41044074-3D7AD2B5-B630-4AA4-B7F3-2C573A66C364Q41074841-8D92F06E-D61C-4489-BB73-E7E49E0D3EA2Q41125260-19F24904-1548-4D49-A10B-34F253FC2EC0Q41315277-A222C4A0-BFFB-4235-8A1E-11E9BDE7529CQ41840749-649EC28B-1803-4022-9F48-7D1D696B2C77Q42048957-2A74BFDD-57DA-4529-B9E9-F585CAEAF1D7Q42158841-0CDEEFA5-1652-41E4-83C4-FFBEEC88C0DDQ42335569-5A39BA48-D35B-4AAE-9C44-EF5C0107B7A9Q43246607-2CCFEB80-1AE1-4AEB-9044-BD7F940FD519Q44685710-0DD20031-10FA-46E9-8BAC-273515D3C9E7Q45141952-B0447A9D-3266-45FD-871B-5300BD318B83Q45359417-947DCE28-BDC3-415A-9FB2-A78C8A2A6651Q45906651-FA644AED-D84D-4C38-B8B7-43C92A4A2EC9Q46655841-98EBFF4F-F6DB-4486-AF9C-534F5938EA42Q47152787-5228B333-A276-4543-A5BE-74814CDC8E98Q47708598-8523BD45-A144-462A-B4AA-4EF4314628E6Q48257064-E305DFDC-7ABD-46A1-AC7D-A65D0D90C6EDQ48296304-9A0E6285-D139-4ACF-A330-0E0227FADDBDQ48313422-0118E658-7823-4098-945B-4FAD09202607Q50941129-B041FC3A-5F8D-41FB-A880-63EC9284D61AQ51102596-F813C1A4-2D03-49AE-8FB5-CE27C1A4646DQ57242523-0946FF6C-4FEB-4645-B2FA-FD8FDB37C77AQ57242555-516D78AD-20C8-41DD-9CD6-248124375AB6Q57705141-FB9BE8DF-38AF-4BE6-8AD4-575B884C3A6BQ58712013-221DB650-4ED3-4B69-AA99-207005918B59Q58778541-6FE12A79-6BD7-41A8-958E-7E7C73322306Q62603789-C1491334-121D-44D1-B1A9-DA6A3E34F956
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
M. Carmen Galan
@ast
M. Carmen Galan
@en
M. Carmen Galan
@es
M. Carmen Galan
@nl
M. Carmen Galan
@sl
type
label
M. Carmen Galan
@ast
M. Carmen Galan
@en
M. Carmen Galan
@es
M. Carmen Galan
@nl
M. Carmen Galan
@sl
prefLabel
M. Carmen Galan
@ast
M. Carmen Galan
@en
M. Carmen Galan
@es
M. Carmen Galan
@nl
M. Carmen Galan
@sl
P1053
G-7858-2012
P106
P21
P31
P3829
P496
0000-0001-7307-2871