Works matching AU García‐Tellado, Fernando
Results: 31
Ab initio crystal structure determination of two chain functionalized pyrroles from synchrotron X-ray powder diffraction data.
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- Powder Diffraction, 2012, v. 27, n. 3, p. 172, doi. 10.1017/S0885715612000498
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Asymmetrische Alkinylierung von Iminen durch Kooperation von Wasserstoffbrücken und Metallkatalyse.
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- Angewandte Chemie, 2010, v. 122, n. 6, p. 1029, doi. 10.1002/ange.200906018
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Solvent-Free Microwave-Assisted Efficient Synthesis of 4,4-Disubstituted 2-Oxazolines.
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 22, p. 4387
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- Article
Stereodiversified Modular Synthesis of Non‐planar Five‐Membered Cyclic N‐Hydroxylamidines: Reactivity Study and Application to the Synthesis of Cyclic Amidines.
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- Advanced Synthesis & Catalysis, 2018, v. 360, n. 22, p. 4362, doi. 10.1002/adsc.201800749
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Asymmetric Alkynylation of Imines by Cooperative Hydrogen Bonding and Metal Catalysis.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 6, p. 1013, doi. 10.1002/anie.200906018
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- Article
Acetylides from Alkyl Propiolates as Building Blocks for C<sub>3</sub> Homologation.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 12, p. 2090, doi. 10.1002/anie.200801987
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Merging Domino and Redox Chemistry: Stereoselective Access to Di- and Trisubstituted β,γ-Unsaturated Acids and Esters.
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- Chemistry - A European Journal, 2012, v. 18, n. 12, p. 3468, doi. 10.1002/chem.201103763
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Diverted Domino Reactivity in Tertiary Skipped Diynes: A Convenient Access to Polyfunctionalized Cyclohexadienones and Multivalent Aromatic Scaffolds.
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- Chemistry - A European Journal, 2011, v. 17, n. 35, p. 9571, doi. 10.1002/chem.201101676
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A Microwave-Assisted Domino Rearrangement of Propargyl Vinyl Ethers to Multifunctionalized Aromatic Platforms.
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- Chemistry - A European Journal, 2011, v. 17, n. 12, p. 3318, doi. 10.1002/chem.201003532
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Tertiary Skipped Diynes: A Pluripotent Building Block for the Modular and Diversity-Oriented Synthesis of Nitrogen Heterocycles.
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- Chemistry - A European Journal, 2010, v. 16, n. 11, p. 3276, doi. 10.1002/chem.200903577
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A Convenient Domino Access to Substituted Alkyl 1,2-Dihydropyridine-3-carboxylates from Propargyl Enol Ethers and Primary Amines.
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- Chemistry - A European Journal, 2010, v. 16, n. 2, p. 428, doi. 10.1002/chem.200902140
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From Conjugated Tertiary Skipped Diynes to Chain-Functionalized Tetrasubstituted Pyrroles.
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- Chemistry - A European Journal, 2009, v. 15, n. 4, p. 838, doi. 10.1002/chem.200802262
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- Article
Dual Reactivity Pattern of Allenolates 'On Water': The Chemical Basis for Efficient Allenolate-Driven Organocatalytic Systems.
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- Chemistry - A European Journal, 2007, v. 13, n. 17, p. 4823, doi. 10.1002/chem.200700227
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A Substrate-Based Folding Process Incorporating Chemodifferentiating ABB′ Three-Component Reactions of Terminal Alkynoates and 1,2-Dicarbonyl Compounds: A Skeletal-Diversity-Oriented Synthetic Manifold.
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- Chemistry - A European Journal, 2007, v. 13, n. 4, p. 1201, doi. 10.1002/chem.200600749
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Hydrogen Bond Controlled Anti-Aza-Michael Addition: Diastereoselective Synthesis of Cyclobutene-Containing Amino Acid Derivatives.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 16, p. 3462, doi. 10.1002/ejoc.201500269
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A Robust and General Protocol for the Lewis-Base-Catalysed Reaction of Alcohols and Alkyl Propiolates.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 1, p. 198, doi. 10.1002/ejoc.201301303
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Reactivity Control in the Addition of N, N′-Dialkylated 1, n-Diamines to Activated Skipped Diynes: Synthesis of Fused Bicyclic 1,4-Diazepanes and 1,5-Diazocanes.
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- European Journal of Organic Chemistry, 2011, v. 2011, n. 34, p. 6847, doi. 10.1002/ejoc.201101368
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SYNTHESIS AND CHEMISTRY OF TETRONIC ACIDS.
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- Organic Preparations & Procedures International, 2004, v. 36, n. 1, p. 33, doi. 10.1080/00304940409355370
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Catalytic Hydrocyanation of Activated Terminal Alkynes.
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- Chemistry - A European Journal, 2019, v. 25, n. 66, p. 15046, doi. 10.1002/chem.201903402
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Synthesis, biological and computational evaluation of novel cyanomethyl vinyl ether derivatives.
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- Frontiers in Pharmacology, 2024, p. 1, doi. 10.3389/fphar.2024.1344042
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Acrylonitrile Derivatives against Trypanosoma cruzi : In Vitro Activity and Programmed Cell Death Study.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 6, p. 552, doi. 10.3390/ph14060552
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A Domino Strategy for the Synthesis of 2H‐Pyrans from Propargyl Vinyl Ethers.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 8, p. 1784, doi. 10.1002/ejoc.201801847
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A Focused Library of NO‐Donor Compounds with Potent Antiproliferative Activity Based on Green Multicomponent Reactions.
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- ChemMedChem, 2019, v. 14, n. 18, p. 1669, doi. 10.1002/cmdc.201900385
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Efficient Domino Process Based on the Catalytic Generation of Non-Metalated, Conjugated Acetylides in the Presence of Aldehydes or Activated Ketones.
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- Chemistry - A European Journal, 2003, v. 9, n. 13, p. 3122, doi. 10.1002/chem.200204579
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Cyanovinylation of Aldehydes: Organocatalytic Multicomponent Synthesis of Conjugated Cyanomethyl Vinyl Ethers.
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- Molecules, 2021, v. 26, n. 14, p. 4120, doi. 10.3390/molecules26144120
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A General and Scalable Synthesis of Polysubstituted Indoles.
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- Molecules, 2020, v. 25, n. 23, p. 5595, doi. 10.3390/molecules25235595
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Recent Advances in the Synthesis of 2H-Pyrans.
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- Molecules, 2019, v. 24, n. 16, p. 2904, doi. 10.3390/molecules24162904
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Integrative Pericyclic Cascade: An Atom Economic, Multi C−C Bond-Forming Strategy for the Construction of Molecular Complexity.
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- Chemistry - A European Journal, 2017, v. 23, n. 42, p. 10048, doi. 10.1002/chem.201702667
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Microwave-Assisted Organocatalyzed Rearrangement of Propargyl Vinyl Ethers to Salicylaldehyde Derivatives: An Experimental and Theoretical Study.
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- Chemistry - A European Journal, 2015, v. 21, n. 50, p. 18280, doi. 10.1002/chem.201503171
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Water-Compatible Hydrogen-Bond Activation: A Scalable and Organocatalytic Model for the Stereoselective Multicomponent Aza-Henry Reaction.
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- Chemistry - A European Journal, 2013, v. 19, n. 49, p. 16550, doi. 10.1002/chem.201303448
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Highly 1,2- trans Stereoselective Allylations of 1,2- O-Isopropylidene-Protected Glycofuranosides.
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- Angewandte Chemie International Edition, 2000, v. 39, n. 15, p. 2727, doi. 10.1002/1521-3773(20000804)39:15<2727::AID-ANIE2727>3.0.CO;2-I
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