about
1,2-Didehydro[10]annulenes: Structures, Aromaticity, and CyclizationsInfluence of solvent and salt concentration on the alignment properties of acrylamide copolymer gels for the measurement of RDC.Conformational analysis of the anti-obesity drug lorcaserin in water: how to take advantage of long-range residual dipolar couplings.Disodium cromoglycate: exploiting its properties as a NMR weak-aligning medium for small organic molecules.Dynamics of the glycosidic bond: conformational space of lactose.Conformational stable alleno-acetylenic cyclophanes bearing chiral axes.Lanthanide-chelating carbohydrate conjugates are useful tools to characterize carbohydrate conformation in solution and sensitive sensors to detect carbohydrate-protein interactions.Challenge of large-scale motion for residual dipolar coupling based analysis of configuration: the case of fibrosterol sulfate A.Computer-Assisted 3D Structure Elucidation of Natural Products using Residual Dipolar Couplings.The binding mode of side chain- and C3-modified epothilones to tubulin.Collection of NMR Scalar and Residual Dipolar Couplings Using a Single Experiment.Potent antiprotozoal activity of a novel semi-synthetic berberine derivative.Probing heterocycle conformation with residual dipolar couplings.Cyclic allene intermediates in intramolecular dehydro Diels-Alder reactions: labeling and theoretical cycloaromatization studies.MSpin-RDC. A program for the use of residual dipolar couplings for structure elucidation of small molecules.MSpin-JCoupling. A modular program for prediction of scalar couplings and fast implementation of Karplus relationships.Mechanical Behavior of Polymer Gels for RDCs and RCSAs Collection: NMR Imaging Study of Buckling Phenomena.Measurement of residual chemical shift anisotropies in compressed polymethylmethacrylate gels. Automatic compensation of gel isotropic shift contribution.Computer-Assisted 3D Structure Elucidation (CASE-3D) of Natural Products Combining Isotropic and Anisotropic NMR Parameters.Experimental and computational exploration of indolizinyl carbene generation. A route to biindolizines.Self-Sensitized Photooxygenation of 2H-Pyrans: Characterization of Unexpected Products Assisted by Computed Structural Elucidation and Residual Dipolar Couplings.Diastereoselectivity in an electrocyclization reaction of cyclopentadienonesDeantiaromatization as a Driving Force in an Electrocyclic ReactionComputational Studies on the Cyclizations of Enediynes, Enyne-Allenes, and Related Polyunsaturated Systems†Cope Reaction Families: To Be or Not to Be a BiradicalPhytochemical Study of Senecio volckmannii Assisted by CASE-3D with Residual Dipolar Couplings and Isotropic H/C NMR Chemical ShiftsIntegrated Ugi-Based Assembly of Functionally, Skeletally, and Stereochemically Diverse 1,4-Benzodiazepin-2-onesIs Enantiomer Assignment Possible by NMR Spectroscopy Using Residual Dipolar Couplings from Chiral Nonracemic Alignment Media?-A Critical AssessmentPreparation and Characterization of a Halogen-Bonded Shape-Persistent Chiral Alleno-acetylenic Inclusion ComplexRotation-Locked 2,6-Pyrido-allenophanes: Characterization of all StereoisomersA study of aryl radical cyclization in enaminone estersStrained intermediates in intramolecular dehydro Diels-Alder reactions: rearrangement of cyclic allenes via 1,2-dehydro[10]annulenesA graphical tool for the prediction of vicinal proton-proton 3J(HH) coupling constantsPreparation of 13C4-6-methyl anthranilic ester via a Diels-Alder-type process. an experimental and theoretical study to characterize an unexpected isotope exchangeResidual dipolar couplings of freely rotating groups in small molecules. Stereochemical assignment and side-chain conformation of 8-phenylmentholUnprecedented stereoselective synthesis of cyclopenta[b]benzofuran derivatives and their characterisation assisted by aligned media NMR and 13C chemical shift ab initio predictionsChiral (2,5)pyrido[7(4)]allenoacetylenic cyclophanes: synthesis and characterizationStereochemistry determination by powder X-ray diffraction analysis and NMR spectroscopy residual dipolar couplingsModeling dinitrogen activation by lithium: a mechanistic investigation of the cleavage of N2 by stepwise insertion into small lithium clustersMechanistic investigation on the formation of indolizines from 2-enynylpyridines
P50
Q29307768-862B6ABD-7240-4336-9A1B-7FEEA59948C5Q30583892-CC949DBC-771C-480C-857B-A533904156F0Q30672639-217D2353-12F9-4518-A7A0-D43193146840Q30758467-C2EE5EE5-40C6-42D1-9DD2-AFC061DE90BBQ33960567-C5BC2531-662C-45AC-8C8F-D59972E9AFB9Q38244463-7E4D39C5-ADC6-4A50-81D3-44D0845010DAQ38307047-5D936054-0854-4CB0-A16A-D5C93CB61A6AQ38434576-4F2C99E1-E80F-4E6E-AB04-B837D1C2BF86Q38937600-4E11477B-EEC3-4059-B4C6-47F8DE3D9B24Q39708874-70667510-54A1-464A-AAAA-6387D9F97871Q40376964-E1A2FFBA-D083-4A05-9C8E-A6B89EE84421Q42743627-C93F2A05-6506-470B-A671-51C26B3BF19BQ42972175-AA4E9651-7A1A-4DAB-8A78-E1A9C373C185Q44331396-4A90DFDF-E969-47BB-A862-D0491C5BBA6EQ46453844-A66422E2-6BA9-4687-8A8A-CE8819767738Q47671934-B5BF40D4-ADC0-4540-8577-04DE2F343C0EQ48255021-884FAA72-7C0B-444E-B625-43CF8CE554D6Q48255824-87505AF4-97EE-4446-A09A-C5EBB7D50633Q48260972-2E38FB98-F3AB-4779-9F01-D072BA0B6FCBQ48275119-E5E22305-94FF-4ABC-98B3-F5593A6B42BFQ52937653-FF41B3DF-896D-42DC-8A95-4AA59BC712EDQ57742935-BCC64809-92E3-47A8-974D-226DAF9C11E1Q57743003-510DAF70-DDE3-4B4A-A3DA-5175A900F209Q57743068-9D545EEB-414B-423C-A3AC-3EC80DD15DA2Q57743106-77A320E2-3FD4-41F8-A133-6301A9B302EBQ57787560-4042905D-1F0E-4B73-9038-F09070FF322AQ60432512-7398B1E6-DAEB-46B2-8221-A8CDE4BA0A65Q63290867-BE9794A2-F444-4221-B3DB-10635717A6F1Q64167027-0979A293-6F21-49C2-AE10-D9D87811B01CQ64167028-FCB70156-4D04-4CEC-BF7C-EF232E801467Q74064023-97CDD625-13C6-466E-AED9-E0073158468EQ74502335-8195CCC0-79B4-435C-B454-704DA2AAD097Q80784379-CADEB96B-88BD-4028-90C9-498549D1D9BBQ81041395-952299F1-294F-4E11-B3C9-6F11EDB44FEAQ83555477-3311FC8B-71D7-4BE2-9A55-A6C8A44D26BBQ83611846-50B5A8F9-D2B7-4EB0-8645-A31C4F7E4759Q83900312-9BEF3485-E2DC-48C1-9D73-F406FE6B926AQ84124910-C1319E32-881E-4554-AD8F-035757E0EB82Q84455624-D4A11AEC-AD4A-42F7-82CE-F9ABBDDEF7ABQ84598770-3E9C3670-45FA-4650-9335-F74E5F6B70CE
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Armando Navarro-Vázquez
@ast
Armando Navarro-Vázquez
@en
Armando Navarro-Vázquez
@es
Armando Navarro-Vázquez
@nl
type
label
Armando Navarro-Vázquez
@ast
Armando Navarro-Vázquez
@en
Armando Navarro-Vázquez
@es
Armando Navarro-Vázquez
@nl
prefLabel
Armando Navarro-Vázquez
@ast
Armando Navarro-Vázquez
@en
Armando Navarro-Vázquez
@es
Armando Navarro-Vázquez
@nl
P106
P1153
6603311426
P21
P31
P496
0000-0003-4364-516X