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Refinado por: assunto: Chemistry remover Base de dados/Biblioteca: Royal Society Of Chemistry Journals 2008- remover
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Enzyme-modified electrodes for biosensors and biofuel cells
Enzyme-modified electrodes for biosensors and biofuel cells
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Enzyme-modified electrodes for biosensors and biofuel cells

Pinyou, Piyanut ; Blay, Vincent ; Muresan, Liana Maria ; Noguer, Thierry

Materials horizons, 2019-08, Vol.6 (7), p.1336-1358 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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2
Highly enantioselective aza-Henry reaction with isatin N-Boc ketimines
Highly enantioselective aza-Henry reaction with isatin N-Boc ketimines
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Highly enantioselective aza-Henry reaction with isatin N-Boc ketimines

Holmquist, Melireth ; Blay, Gonzalo ; Pedro, José R

Chemical communications (Cambridge, England), 2014-08, Vol.50 (66), p.9309-9312 [Periódico revisado por pares]

England

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3
Subnanometric Pt clusters dispersed over Cs-doped TiO2 for CO2 upgrading via low-temperature RWGS: operando mechanistic insights to guide an optimal catalyst design
Subnanometric Pt clusters dispersed over Cs-doped TiO2 for CO2 upgrading via low-temperature RWGS: operando mechanistic insights to guide an optimal catalyst design
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Subnanometric Pt clusters dispersed over Cs-doped TiO2 for CO2 upgrading via low-temperature RWGS: operando mechanistic insights to guide an optimal catalyst design

Torres-Sempere, Guillermo ; Blay-Roger, Rubén ; Luque-Álvarez, Ligia A ; Santos, José L ; Bobadilla, Luis F ; Pastor-Pérez, Laura ; Centeno, Miguel A ; Hernández, Willinton Y ; Ibraheem Yousef ; Odriozola, José A ; Reina, Tomas R

Journal of materials chemistry. A, Materials for energy and sustainability, 2024-01, Vol.12 (3), p.1779-1792 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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4
Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis
Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis
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Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis

Martínez-Pardo, Pablo ; Blay, Gonzalo ; Muñoz, M Carmen ; Pedro, José R ; Sanz-Marco, Amparo ; Vila, Carlos

Chemical communications (Cambridge, England), 2018, Vol.54 (23), p.2862-2865 [Periódico revisado por pares]

England: Royal Society of Chemistry

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5
Dual dean entrainment with volume ratio modulation for efficient droplet co-encapsulation: extreme single-cell indexing
Dual dean entrainment with volume ratio modulation for efficient droplet co-encapsulation: extreme single-cell indexing
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Dual dean entrainment with volume ratio modulation for efficient droplet co-encapsulation: extreme single-cell indexing

Harrington, Jack ; Esteban, Luis Blay ; Butement, Jonathan ; Vallejo, Andres F ; Lane, Simon I. R ; Sheth, Bhavwanti ; Jongen, Maaike S. A ; Parker, Rachel ; Stumpf, Patrick S ; Smith, Rosanna C. G ; MacArthur, Ben D ; Rose-Zerilli, Matthew J. J ; Polak, Marta E ; Underwood, Tim ; West, Jonathan

Lab on a chip, 2021-09, Vol.21 (17), p.3378-3386 [Periódico revisado por pares]

England: Royal Society of Chemistry

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6
Visible-light-accelerated amination of quinoxalin-2-ones and benzo[1,4]oxazin-2-ones with dialkyl azodicarboxylates under metal and photocatalyst-free conditions
Visible-light-accelerated amination of quinoxalin-2-ones and benzo[1,4]oxazin-2-ones with dialkyl azodicarboxylates under metal and photocatalyst-free conditions
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Visible-light-accelerated amination of quinoxalin-2-ones and benzo[1,4]oxazin-2-ones with dialkyl azodicarboxylates under metal and photocatalyst-free conditions

Rostoll-Berenguer, Jaume ; Capella-Argente, Murta ; Blay, Gonzalo ; Pedro, José R ; Vila, Carlos

Organic & biomolecular chemistry, 2021-07, Vol.19 (28), p.625-6255 [Periódico revisado por pares]

England: Royal Society of Chemistry

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7
Theta-1 zeolite catalyst for increasing the yield of propene when cracking olefins and its potential integration with an olefin metathesis unit
Theta-1 zeolite catalyst for increasing the yield of propene when cracking olefins and its potential integration with an olefin metathesis unit
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Theta-1 zeolite catalyst for increasing the yield of propene when cracking olefins and its potential integration with an olefin metathesis unit

Blay, Vincent ; Miguel, Pablo J. ; Corma, Avelino

Catalysis science & technology, 2017, Vol.7 (24), p.5847-5859 [Periódico revisado por pares]

Cambridge: Royal Society of Chemistry

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8
Catalytic asymmetric conjugate addition of terminal alkynes to β-trifluoromethyl α,β-enones
Catalytic asymmetric conjugate addition of terminal alkynes to β-trifluoromethyl α,β-enones
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Catalytic asymmetric conjugate addition of terminal alkynes to β-trifluoromethyl α,β-enones

Sanz-Marco, Amparo ; García-Ortiz, Andrea ; Blay, Gonzalo ; Pedro, José R

Chemical communications (Cambridge, England), 2014-03, Vol.50 (18), p.2275-2278 [Periódico revisado por pares]

England

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9
Organocatalytic enantioselective Mannich reaction of isoxazol-5(4)-ones to isatin-derived ketimines
Organocatalytic enantioselective Mannich reaction of isoxazol-5(4)-ones to isatin-derived ketimines
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Organocatalytic enantioselective Mannich reaction of isoxazol-5(4)-ones to isatin-derived ketimines

Torán, Ricardo ; Puchán, Dario ; Sanz-Marco, Amparo ; Vila, Carlos ; Pedro, José R ; Blay, Gonzalo

Organic & biomolecular chemistry, 2022-11, Vol.2 (43), p.8395-8399 [Periódico revisado por pares]

England: Royal Society of Chemistry

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10
Enantioselective construction of quaternary stereocenters via organocatalytic arylation of isoxazolin-5-ones with o -quinone diimides
Enantioselective construction of quaternary stereocenters via organocatalytic arylation of isoxazolin-5-ones with o -quinone diimides
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Enantioselective construction of quaternary stereocenters via organocatalytic arylation of isoxazolin-5-ones with o -quinone diimides

Torán, Ricardo ; Portillo, Eduardo ; Sanz-Marco, Amparo ; Vila, Carlos ; Blay, Gonzalo

Organic Chemistry Frontiers, 2023-12, Vol.10 (24), p.6081-6086 [Periódico revisado por pares]

London: Royal Society of Chemistry

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