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- (3R,4S,5R,6R,7S)-3,4,5,7-Tetrahydroxyconidine, an azetidine analogue of 6,7-diepicastanospermine and a conformationally constrained D- deoxyaltronojirimycin, from L-arabinose
- A Novel Agonist of the Type 1 Lysophosphatidic Acid Receptor (LPA<inf>1</inf>), UCM-05194, Shows Efficacy in Neuropathic Pain Amelioration
- A quantitative structure-reactivity relationship in N-acetyl oxazolidines: An electrostatic interaction controls rotamer population
- An Eco-Friendly and Switchable Carbon-Based Catalyst for Protection-Deprotection of Vicinal Diols
- An anomeric effect drives the regiospecific ring-opening of 1,3-oxazolidines under acetylating conditions
- An efficient and highly diastereoselective synthesis of C-glycosylated 1,3-oxazolidines from N-methyl-d-glucamine
- Azetidine iminosugars from the cyclization of 3,5-Di- O -triflates of α-furanosides and of 2,4-Di- O -triflates of β-pyranosides derived from glucose
- C-branched iminosugars: α-glucosidase inhibition by enantiomers of isoDMDP, isoDGDP, and isoDAB- l -isoDMDP compared to miglitol and miglustat
- Carbohydrate derived bicyclic azetidin-3-ones as scaffolds for highly functionalized azetidines
- Cycloadditions with mesoionic dipoles: Strategy and control
- Discovery and mechanism of action studies of 4,6-diphenylpyrimidine-2-carbohydrazides as utrophin modulators for the treatment of Duchenne muscular dystrophy
- Glycosidase inhibition by all 10 stereoisomeric 2,5-dideoxy-2,5- iminohexitols prepared from the enantiomers of glucuronolactone
- Hydrazones from hydroxy naphthaldehydes. Part 2. Condensations with aromatic N-aminoheterocycles and elucidation of tautomeric structures
- Hydrazones from hydroxy naphthaldehydes and N-aminoheterocycles: Structure and stereodynamics
- Imine or Enamine? Insights and Predictive Guidelines from the Electronic Effect of Substituents in H-Bonded Salicylimines
- Isolation from Stevia rebaudiana of DMDP acetic acid, a novel iminosugar amino acid: synthesis and glycosidase inhibition profile of glycine and β-alanine pyrrolidine amino acids
- Mechanistic Insights into the Oxidative Degradation of Formic and Oxalic Acids with Ozone and OH Radical. A Computational Rationale
- Mutarotation of aldoses: Getting a deeper knowledge of a classic equilibrium enabled by computational analyses
- N-(2-Carboxyethyl)-2,5-dideoxy-2,5-imino-D-mannonic acid [(3R,4R,5R)-1-(2-carboxyethyl)-3,4-dihydroxy-5-hydroxymethyl-L-proline]
- Nine of 16 stereoisomeric polyhydroxylated proline amides are potent β-N-acetylhexosaminidase inhibitors
- Novel Antagonist of the Type 2 Lysophosphatidic Acid Receptor (LPA<inf>2</inf>), UCM-14216, Ameliorates Spinal Cord Injury in Mice
- On the Origin of Sugar Handedness: Facts, Hypotheses and Missing Links-A Review
- Organic Sonochemistry: A Chemist's Timely Perspective on Mechanisms and Reactivity
- Schiff bases from TRIS and formylpyridines: Structure and mechanistic rationale aided by DFT calculations
- Schiff bases from TRIS and ortho-hydroxyarenecarbaldehydes: Structures and tautomeric equilibria in the solid state and in solution
- Short and sweet: D-glucose to L-glucose and L-glucuronic acid
- Structural essentials for β-: N -acetylhexosaminidase inhibition by amides of prolines, pipecolic and azetidine carboxylic acids
- Synthesis from d-altrose of (5 R,6 R,7 R,8 S)-5,7-dihydroxy-8- hydroxymethylconidine and 2,4-dideoxy-2,4-imino-d-glucitol, azetidine analogues of swainsonine and 1,4-dideoxy-1,4-imino-d-mannitol
- Synthesis of the enantiomers of XYLNAc and LYXNAc: Comparison of β-N-acetylhexosaminidase inhibition by the 8 stereoisomers of 2-N-acetylamino-1,2,4-trideoxy-1,4-iminopentitols
- Targeting the FtsZ Allosteric Binding Site with a Novel Fluorescence Polarization Screen, Cytological and Structural Approaches for Antibacterial Discovery
- Tautomerism in Schiff bases. the cases of 2-hydroxy-1-naphthaldehyde and 1-hydroxy-2-naphthaldehyde investigated in solution and the solid state
- The Dimroth rearrangement as a probable cause for structural misassignments in imidazo[1,2-a]pyrimidines: A <sup>15</sup>N-labelling study and an easy method for the determination of regiochemistry
- The structural assembly switch of cell division protein FtsZ probed with fluorescent allosteric inhibitors
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