about
Mitotic arrest induced by a novel family of DNA topoisomerase II inhibitors.Chemo-differentiating ABB' multicomponent reactions. Privileged building blocks.Tertiary skipped diynes: a pluripotent building block for the modular and diversity-oriented synthesis of nitrogen heterocycles.A convenient domino access to substituted alkyl 1,2-dihydropyridine-3-carboxylates from propargyl enol ethers and primary amines.An effective one-pot synthesis of 5-substituted tetronic acids.Efficient domino process based on the catalytic generation of non-metalated, conjugated acetylides in the presence of aldehydes or activated ketones.A modular, one-pot, four-component synthesis of polysubstituted 1,3-oxazolidines.Synthesis of fully substituted pyrimidines.Ambiphilic allenes: synthesis and reactivity.Diversifying Complexity by Domino Benzannulation of Polycyclic Natural Products.Integrative Pericyclic Cascade: An Atom Economic, Multi C-C Bond-Forming Strategy for the Construction of Molecular Complexity.Microwave-assisted domino access to C2-chain functionalized furans from tertiary propargyl vinyl ethers.Organocatalysis "on water". Regioselective [3 + 2]-cycloaddition of nitrones and allenolates.Alkynoates as a source of reactive alkylinides for aldehyde addition reactionsHighly 1,2-trans Stereoselective Allylations of 1,2-O-Isopropylidene-Protected Glycofuranosides This work was supported by the Canary Islands Consejería de Educación y Ciencia (PI1998/109), the Spanish Comisión Interministerial de Ciencia y TecnologA substrate-based folding process incorporating chemodifferentiating ABB' three-component reactions of terminal alkynoates and 1,2-dicarbonyl compounds: a skeletal-diversity-oriented synthetic manifoldChemo-differentiating MCRs based on alpha-ketoesters and terminal alkynoates. A homoaldol-based ABB' systemDual reactivity pattern of allenolates "on water": the chemical basis for efficient allenolate-driven organocatalytic systemsA diversity-oriented strategy for the construction of tetrasubstituted pyrroles via coupled domino processesMetal-free access to fully substituted skipped diynes. An efficient chemodifferentiating A2BB' 4CR manifoldA convenient and chemoselective one-pot oxidation/Wittig reaction for the C2-homologation of carbohydrate-derived glycolsMulticomponent domino processes based on the organocatalytic generation of conjugated acetylides: efficient synthetic manifolds for diversity-oriented molecular constructionAsymmetric alkynylation of imines by cooperative hydrogen bonding and metal catalysisFrom conjugated tertiary skipped diynes to chain-functionalized tetrasubstituted pyrrolesA microwave-assisted domino rearrangement of propargyl vinyl ethers to multifunctionalized aromatic platformsMerging domino and redox chemistry: stereoselective access to di- and trisubstituted β,γ-unsaturated acids and estersDiverted domino reactivity in tertiary skipped diynes: a convenient access to polyfunctionalized cyclohexadienones and multivalent aromatic scaffoldsWater-compatible hydrogen-bond activation: a scalable and organocatalytic model for the stereoselective multicomponent aza-Henry reactionPropargyl Claisen rearrangement: allene synthesis and beyondCatalytic Hydrocyanation of Activated Terminal AlkynesSynthesis and Utility of 2,2-Dimethyl-2 H-pyrans: Dienes for Sequential Diels-Alder/Retro-Diels-Alder ReactionsA Focused Library of NO-Donor Compounds with Potent Antiproliferative Activity Based on Green Multicomponent Reactions
P50
Q33560233-AC923C6D-6BC7-4611-9D44-7DBA3AFC3B72Q36746383-9A825221-74DB-4EEA-8181-3A36C4A21B96Q43154369-AACF0C0B-2311-4BFD-8E6E-81F98D20714DQ43239800-0E236ED3-8989-408A-A790-E3B9CB81D60CQ44399404-9EB8D9C6-45A0-4F09-9762-0516FAC964B0Q44495954-2F90595F-D643-4E06-9312-6AA7068403D6Q45241505-A536CB57-3E70-4830-B11C-827D5D33AD79Q45603679-2C8148DA-BEE6-4044-AC01-F3329ED2EAF9Q46045350-E913089B-F247-4511-93FE-A9A17EE59A5CQ48200089-6CCEB157-9DBA-4380-A43B-CE7F4952D4F3Q48266954-719A3905-A2D6-4B3B-A81D-5FC3F165CAEBQ50601802-AEA119E1-9096-4E83-A499-592B35E8FF6EQ52672762-FF2F7CB3-D1F6-4DC1-9B27-E682F88CDDADQ74018715-69F0ACD5-8C29-408F-B100-DFDEE74E1B24Q74140269-7A924211-7579-46F8-9C0B-D2E6617B33F8Q79318228-85A18EE1-ADA3-4916-86AC-993288C5150AQ79755975-3D45111E-46FB-45C0-8EBD-173F15CB1359Q80196703-D08D08B2-FC04-4507-AFB8-B8CCC540E0E3Q80295695-00EB0FCA-627A-4DDC-BCEA-D95AEE3A8298Q80455879-15D096A9-683E-4C75-B469-C25C4572D072Q81489911-DC381783-D3E1-4AEE-8F9C-B1D5285AEBA4Q81491804-10574E46-A540-4783-81E1-0EC7842494FAQ82356892-88DDA625-2D30-4832-B55D-BEC4D784560AQ82984258-AD3E3A2E-C15A-4FE8-8745-FFE514F510F2Q83427824-33F93018-7963-4F55-A0E1-73E58D1D7E62Q83485282-88E0AB9B-2FC0-418D-BBD7-DCEA174E5C21Q84598463-D9D10FC4-260B-4E70-9547-948DA2ADF18DQ86853775-7C993391-7509-4802-B95C-291A8D7842FDQ87407893-24C76399-0E75-4A41-A710-EDDA2155FC23Q90274417-FAADE886-4857-4FCB-8293-C9A669D5FE04Q90331988-ABD8AFA0-C821-4E9B-BD1A-DECCD3F6F0BDQ92252830-56ED7CE0-BBC5-4FEE-9C88-7A7569B67ACF
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Fernando García-Tellado
@ast
Fernando García-Tellado
@en
Fernando García-Tellado
@es
Fernando García-Tellado
@nl
Fernando García-Tellado
@sl
type
label
Fernando García-Tellado
@ast
Fernando García-Tellado
@en
Fernando García-Tellado
@es
Fernando García-Tellado
@nl
Fernando García-Tellado
@sl
altLabel
Fernando G. Tellado
@en
Fernando GarciaTellado
@en
prefLabel
Fernando García-Tellado
@ast
Fernando García-Tellado
@en
Fernando García-Tellado
@es
Fernando García-Tellado
@nl
Fernando García-Tellado
@sl
P1053
J-6037-2014
P106
P1153
6602466196
P21
P31
P3829
P496
0000-0001-6470-6289