Menéndez, J. Carlos.
Menéndez, J. Carlos (José Carlos)
Menéndez Ramos, José Carlos
J. Carlos Menéndez researcher
VIAF ID: 64339751 (Personal)
Permalink: http://viaf.org/viaf/64339751
Preferred Forms
- 100 0 _ ‡a J. Carlos Menéndez ‡c researcher
- 200 _ | ‡a Menéndez ‡b J. Carlos
- 100 1 _ ‡a Menéndez, J. Carlos
- 100 1 _ ‡a Menéndez, J. Carlos
-
- 100 1 _ ‡a Menéndez, J. Carlos ‡q (José Carlos)
-
-
- 100 1 0 ‡a Menéndez Ramos, José Carlos
- 100 1 _ ‡a Menéndez, J. Carlos
-
4xx's: Alternate Name Forms (15)
5xx's: Related Names (1)
Works
Title | Sources |
---|---|
Analytical applications of retinoid-cyclodextrin inclusion complexes. 1. Characterization of a retinal-beta-cyclodextrin complex. | |
Antioxidant, Anti-inflammatory and Neuroprotective Profiles of Novel 1,4-Dihydropyridine Derivatives for the Treatment of Alzheimer's Disease | |
Antioxidants as Molecular Probes: Structurally Novel Dihydro-m-Terphenyls as Turn-On Fluorescence Chemodosimeters for Biologically Relevant Oxidants | |
Axial chirality of 4-arylpyrazolo[3,4-b]pyridines. Conformational analysis and absolute configuration | |
Azaespiro derivados de benzo[a] quinolizidina, antagonistas potenciales de adrenoceptores [alfa]2 | |
B-ring-aryl substituted luotonin A analogues with a new binding mode to the topoisomerase 1-DNA complex show enhanced cytotoxic activity. | |
Brief, efficient and highly diastereoselective synthesis of (±)-pumiliotoxin C based on the generation of an octahydroquinoline precursor via a four-component reaction | |
A catalyst-free multicomponent domino sequence for the diastereoselective synthesis of (E)-3-[2-arylcarbonyl-3-(arylamino)allyl]chromen-4-ones | |
Cerium(IV) ammonium nitrate is an excellent, general catalyst for the Friedländer and Friedländer-Borsche quinoline syntheses: very efficient access to the antitumor alkaloid luotonin A | |
Changes in the reactivity of the fluorescent reagents carbazole-9-carbonyl chloride and 9-carbazolylacetic acid in the presence of cyclodextrins | |
Discovery of a class of diketopiperazines as antiprion compounds. | |
Eco-friendly liquid chromatographic separations based on the use of cyclodextrins as mobile phase additives | |
Efficient synthesis of N-prenylpyrroloindoline and N-prenylindole alkaloids based on a new four-reaction anionic domino process | |
An efficient synthesis of N-substituted 3-nitrothiophen-2-amines. | |
Environmental effects on the fluorescence behaviour of carbazole derivatization reagents. | |
Expedient, catalyst-free, three-component synthesis of fused tetrahydropyridines in water | |
Expedient, one-pot preparation of fused indoles via CAN-catalyzed three-component domino sequences and their transformation into polyheterocyclic compounds containing pyrrolo[1,2-a]azepine fragments | |
A facile three-component [3+2]-cycloaddition/annulation domino protocol for the regio- and diastereoselective synthesis of novel penta- and hexacyclic cage systems, involving the generation of two heterocyclic rings and five contiguous stereocenters | |
The first aza Diels-Alder reaction involving an alpha,beta-unsaturated hydrazone as the dienophile: stereoselective synthesis of C-4 functionalized 1,2,3,4-tetrahydroquinolines containing a quaternary stereocenter | |
Fluorescence properties of the anti-tumour alkaloid luotonin A and new synthetic analogues: pH modulation as an approach to their fluorimetric quantitation in biological samples | |
A Fluorescent Styrylquinoline with Combined Therapeutic and Diagnostic Activities against Alzheimer's and Prion Diseases | |
The Hantzsch Pyrrole Synthesis: Non-conventional Variations and Applications of a Neglected Classical Reaction | |
Heterogeneous Amberlyst-15-catalyzed synthesis of complex hybrid heterocycles containing [1,6]-naphthyridine under metal-free green conditions | |
Identification of 4,6-diaryl-1,4-dihydropyridines as a new class of neuroprotective agents | |
Imaging of β-amyloid plaques by near infrared fluorescent tracers: a new frontier for chemical neuroscience | |
Medicinal chemistry of anticancer drugs | |
Montmorillonite clay-promoted, solvent-free cross-aldol condensations under focused microwave irradiation. | |
Multicomponent Domino Synthesis, Anticancer Activity and Molecular Modeling Simulation of Complex Dispirooxindolopyrrolidines. | |
New 5-unsubstituted dihydropyridines with improved CaV1.3 selectivity as potential neuroprotective agents against ischemic injury | |
A new route toward 4-substituted pyrazino[2,1-b]quinazoline-3,6-dione systems. Total synthesis of glyantrypine | |
One-Pot Access to a Library of Dispiro Oxindole-pyrrolidine/pyrrolothiazole-thiochromane Hybrids via Three-Component 1,3-Dipolar Cycloaddition Reactions | |
A one-pot sequence for the efficient synthesis of highly functionalized macrocarbocycles or bridged 2,8-dioxabicyclo[3.2.1]octanes from 1-nitrobicyclic compounds | |
One-Pot Synthesis of Functionalized Carbazoles via a CAN-Catalyzed Multicomponent Process Comprising a C-H Activation Step. | |
Oxidant-free, three-component synthesis of 7-amino-6H-benzo[c]chromen-6-ones under green conditions | |
Palladium(II)-catalyzed intramolecular carboxypalladation-olefin insertion cascade: direct access to indeno[1,2-b]furan-2-ones | |
Peptidomimetics in cancer chemotherapy. | |
Privileged scaffolds in synthesis: 2,5-piperazinediones as templates for the preparation of structurally diverse heterocycles. | |
Progress in the Chemistry of Tetrahydroquinolines | |
Quantitative determination of dimethicone in commercial tablets and capsules by Fourier transform infrared spectroscopy and antifoaming activity test | |
Recent advances in the synthesis of pyrroles by multicomponent reactions. | |
La síntesis orgánica en la era de los fármacos biológicos : discurso del Excmo. Sr. D. José Carlos Menéndez Ramos leído en la sesión del día 11 de octubre de 2018 para su ingreso como académico de número y contestación de la Excma. Sra. Dña. María del Carmen Avendaño López | |
Spirooxindole-pyrrolidine heterocyclic hybrids promotes apoptosis through activation of caspase-3 | |
Stereoselective synthesis of bicyclo[4.2.1]nonane skeletons by ring-closing metathesis: a new versatile methodology for the efficient assembly of functionalized cyclooctanoids | |
Structure-activity relationships and mechanistic studies of novel mitochondria-targeted, leishmanicidal derivatives of the 4-aminostyrylquinoline scaffold | |
Sustainable Access to Acridin-9-(10<i>H</i>)ones with an Embedded <i>m</i>-Terphenyl Moiety Based on a Three-Component Reaction | |
A Sustainable Approach to the Stereoselective Synthesis of Diazaheptacyclic Cage Systems Based on a Multicomponent Strategy in an Ionic Liquid. | |
Synthesis of 5,6-Dihydrodibenzo[b,h][1,6]naphthyridines via Copper Bromide Catalyzed Intramolecular [4 + 2] Hetero-Diels-Alder Reactions. | |
Synthesis of 6,12-Epiminodibenzo[b,f][1,5]diazocines via an Ytterbium Triflate-Catalyzed, AB2 Three-Component Reaction | |
Synthesis of benzo- and naphtho-fused bicyclo[n.3.1]alkane frameworks with a bridgehead nitrogen function by palladium-catalyzed intramolecular α'-arylation of α-nitroketones | |
Synthesis of polysubstituted, functionalized quinolines through a metal-free domino process involving a C4–C3 functional group rearrangement | |
Synthesis of the quinocarcin core through catalyst-free generation of azomethine ylides | |
A systematic 1 H- and 13 C-NMR spectral analysis of bicyclo[n.3.1]alkanone systems: Determination of the relative configuration of the stereogenic centres and conformation of the six-membered ring. | |
Tetrahydroisoquinoline-Derived Urea and 2,5-Diketopiperazine Derivatives as Selective Antagonists of the Transient Receptor Potential Melastatin 8 (TRPM8) Channel Receptor and Antiprostate Cancer Agents. | |
Three-component access to pyrroles promoted by the CAN-silver nitrate system under high-speed vibration milling conditions: a generalization of the Hantzsch pyrrole synthesis | |
Three-Component Synthesis of a Library of m-Terphenyl Derivatives with Embedded β-Aminoester Moieties | |
Three-component synthesis of highly functionalized aziridines containing a peptide side chain and their one-step transformation into β-functionalized α-ketoamides | |
Two-step stereocontrolled synthesis of densely functionalized cyclic beta-aminoesters containing four stereocenters, based on a new cerium(IV) ammonium nitrate catalyzed sequential three-component reaction | |
Unique Michael addition-initiated domino reaction for the stereoselective synthesis of functionalized macrolactones from alpha-nitroketones in water. | |
Vinylation of nitro-substituted indoles, quinolinones, and anilides with grignard reagents. |