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Regio- and stereoselective synthesis of acetallic tetrahydropyrans as building blocks for natural products preparation, via a tandem [4+3]-cycloaddition/ozonolysis Process
Regio- and stereoselective synthesis of acetallic tetrahydropyrans as building blocks for natural products preparation, via a tandem [4+3]-cycloaddition/ozonolysis Process
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Regio- and stereoselective synthesis of acetallic tetrahydropyrans as building blocks for natural products preparation, via a tandem [4+3]-cycloaddition/ozonolysis Process

Montaña Pedrero, Ángel-Manuel ; Corominas, Albert (Corominas Tarruella) ; Chesa, J.F ; García, F ; Bardia, Ma. Mercedes

Wiley-VCH 2016-08

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Pyridoacridines in the 21st Century
Pyridoacridines in the 21st Century
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Pyridoacridines in the 21st Century

Joule, John A ; Álvarez Domingo, Mercedes

Wiley-VCH 2019-05

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3
Pyridoacridines in the 21st Century
Pyridoacridines in the 21st Century
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Pyridoacridines in the 21st Century

Joule, John A. ; Álvarez, Mercedes

European journal of organic chemistry, 2019-09, Vol.2019 (31-32), p.5043-5072 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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Stereocontrolled annulations of indolo[2,3-a]quinolizidine-derived lactams with a silylated Nazarov reagent. Access to allo and epiallo yohimbine-type derivatives
Stereocontrolled annulations of indolo[2,3-a]quinolizidine-derived lactams with a silylated Nazarov reagent. Access to allo and epiallo yohimbine-type derivatives
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Stereocontrolled annulations of indolo[2,3-a]quinolizidine-derived lactams with a silylated Nazarov reagent. Access to allo and epiallo yohimbine-type derivatives

Arioli, Federica ; Pérez Bosch, Maria ; Are, Celeste ; Estarellas, Carolina ; Luque Garriga, F. Xavier ; Bosch Cartes, Joan ; Amat Tusón, Mercedes

Wiley-VCH 2015-09

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5
Synthesis of (E)-4-bromo-3-methoxybut-3-en-2-one, the key fragment in the polyhydroxylated chain common to oscillariolide and phormidolides A-C
Synthesis of (E)-4-bromo-3-methoxybut-3-en-2-one, the key fragment in the polyhydroxylated chain common to oscillariolide and phormidolides A-C
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Synthesis of (E)-4-bromo-3-methoxybut-3-en-2-one, the key fragment in the polyhydroxylated chain common to oscillariolide and phormidolides A-C

Gil, Alejandro ; Lamariano Merketegi, Janire ; Lorente Crivillé, Adriana ; Albericio Palomera, Fernando ; Álvarez Domingo, Mercedes

Wiley-VCH 2016-05

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6
Origin of the Base-Dependent Facial Selectivity in Annulation Reactions of Nazarov-Type Reagents with Unsaturated Indolo[2,3-a] quinolizidine Lactams
Origin of the Base-Dependent Facial Selectivity in Annulation Reactions of Nazarov-Type Reagents with Unsaturated Indolo[2,3-a] quinolizidine Lactams
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Origin of the Base-Dependent Facial Selectivity in Annulation Reactions of Nazarov-Type Reagents with Unsaturated Indolo[2,3-a] quinolizidine Lactams

Estarellas, Carolina ; Arioli, Federica ; Pérez Bosch, Maria ; Are, Celeste ; Hevia, David ; Molins i Grau, Elies ; Luque Garriga, F. Xavier ; Bosch Cartes, Joan ; Amat Tusón, Mercedes

Wiley-VCH 2017-07

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Origin of the Base-Dependent Facial Selectivity in Annulation Reactions of Nazarov-Type Reagents with Unsaturated Indolo[2,3-a] quinolizidine Lactams
Origin of the Base-Dependent Facial Selectivity in Annulation Reactions of Nazarov-Type Reagents with Unsaturated Indolo[2,3-a] quinolizidine Lactams
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Origin of the Base-Dependent Facial Selectivity in Annulation Reactions of Nazarov-Type Reagents with Unsaturated Indolo[2,3-a] quinolizidine Lactams

Estarellas, Carolina ; Arioli, Federica ; Pérez Bosch, Maria ; Are, Celeste ; Hevia, David ; Molins i Grau, Elies ; Luque Garriga, F. Xavier ; Bosch Cartes, Joan ; Amat Tusón, Mercedes

European journal of organic chemistry, 2017-07 [Periódico revisado por pares]

Wiley-VCH

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8
Novel thermal curing of cycloaliphatic resins by thiol–epoxy click process with several multifunctional thiols
Novel thermal curing of cycloaliphatic resins by thiol–epoxy click process with several multifunctional thiols
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Novel thermal curing of cycloaliphatic resins by thiol–epoxy click process with several multifunctional thiols

Guzmán, Dailyn ; Mateu, Blai ; Fernández‐Francos, Xavier ; Ramis, Xavier ; Serra, Angels

Polymer international, 2017-12, Vol.66 (12), p.1697-1707 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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9
A General Approach To Fabricate Fe3O4 Nanoparticles Decorated with Pd, Au, and Rh: Magnetically Recoverable and Reusable Catalysts for Suzuki CC Cross-Coupling Reactions, Hydrogenation, and Sequential Reactions
A General Approach To Fabricate Fe3O4 Nanoparticles Decorated with Pd, Au, and Rh: Magnetically Recoverable and Reusable Catalysts for Suzuki CC Cross-Coupling Reactions, Hydrogenation, and Sequential Reactions
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A General Approach To Fabricate Fe3O4 Nanoparticles Decorated with Pd, Au, and Rh: Magnetically Recoverable and Reusable Catalysts for Suzuki CC Cross-Coupling Reactions, Hydrogenation, and Sequential Reactions

Gonzàlez de Rivera, Ferran ; Angurell, Inmaculada ; Rossell, Marta D. ; Erni, Rolf ; Llorca, Jordi ; Divins, Núria J. ; Muller, Guillermo ; Seco, Miquel ; Rossell, Oriol

Chemistry : a European journal, 2013-09, Vol.19 (36), p.11963-11974 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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10
A strategy for the triarylation of pyrrolopyrimidines by using microwave-promoted cross-coupling reactions
A strategy for the triarylation of pyrrolopyrimidines by using microwave-promoted cross-coupling reactions
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A strategy for the triarylation of pyrrolopyrimidines by using microwave-promoted cross-coupling reactions

Prieur, Vanessa ; Pujol Dilmé, M. Dolors ; Guillaumet, Gérald

Wiley-VCH 2015-09

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