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ChemCatChem, ISSN 1867-3880, 08/2019, Volume 11, Issue 15, pp. 3341 - 3342
Miquel A. Pericàs was interviewed in celebration of his Gold Medal of the Spanish Royal Society of Chemistry (RSEQ... 
CHEMISTRY, PHYSICAL
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 12/2016, Volume 22, Issue 50, pp. 18247 - 18253
The effect of long‐alkyl‐chain amines in CuI‐assisted azide–alkyne cycloadditions of terminal alkynes with organic azides in glycerol and other environmentally... 
copper | long-chain amines | nanoparticles | azide–alkyne cycloaddition | glycerol | RUTHENIUM NANOPARTICLES | CUAAC | COMPLEXES | COORDINATION | azide-alkyne cycloaddition | PALLADIUM NANOPARTICLES | CHEMISTRY, MULTIDISCIPLINARY | LIGANDS | CHEMISTRY | IONIC LIQUIDS | Glycerin | Nanoparticles | Glycerol | Analysis | Solvents | Cycloaddition | Transmission electron microscopy | Amines | Catalysts | Ingredients | Glycerols | Coure | Nanopartícules | Copper
Journal Article
European journal of organic chemistry, ISSN 1434-193X, 2015, Volume 2015, Issue 6, pp. 1173 - 1188
Journal Article
ACS Catalysis, ISSN 2155-5435, 10/2017, Volume 7, Issue 10, pp. 7008 - 7013
We report a methodology for the catalytic asymmetric cross-coupling of two C­(sp3)–H bonds employing visible light as an economical and environmentally benign... 
DFT | Coupling | Asymmetric catalysis | Organocatalysis | Photoredox | Mechanism | organocatalysis | coupling | ACID | TERTIARY-AMINES | ALPHA-ALKYLATION | CHEMISTRY, PHYSICAL | asymmetric catalysis | photoredox | mechanism | H BOND FUNCTIONALIZATION | DUAL CATALYSIS
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 12/2018, Volume 140, Issue 50, pp. 17349 - 17355
The nickel-catalyzed synthesis of tetrasubstituted cyclobutenes from alkynes is reported. This transformation is uniquely promoted by the use of a primary... 
CYCLIZATIONS | HYDROGENATION | COUPLING REACTIONS | CYCLOBUTENES | RING | COMPLEXES | C-C | DIMERIZATION | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | ALPHA-TRUXILLIC ACID | Phosphines - chemistry | Models, Chemical | Nickel - chemistry | Oxidation-Reduction | Ligands | Alkynes - chemistry | Catalysis | Cycloaddition Reaction | Cyclobutanes - chemical synthesis
Journal Article
FRONTIERS IN PLANT SCIENCE, ISSN 1664-462X, 01/2020, Volume 10
...Author(s): Miquel a. Conesa, Mateu Fullana-Pericas, Antonio Granell, Jeroni Galmes The Mediterranean long shelf-life (LSL) tomatoes are a group of landraces... 
CARBON-ISOTOPE DISCRIMINATION | FRUIT-QUALITY | GROWN TOMATO | STORAGE TOMATO | Mediterranean landraces | tomato | gas exchange | TRADITIONAL VARIETIES | ALCOBACA RIPENING MUTANT | PLANT SCIENCES | yield | WATER-USE EFFICIENCY | drought tolerance | extended fruit shelf-life | DIVERSITY | fruit quality traits | GAS-EXCHANGE
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2014, Volume 53, Issue 36, pp. 9613 - 9616
The development of enantioselective catalytic processes that make use of sunlight as the energy source and nontoxic, affordable materials as catalysts... 
organocatalysis | alkylation | visible light | bismuth oxide | photocatalysis | KETONES | BISMUTH COMPOUNDS | AMINES | ALPHA-ALKYLATION | CHEMISTRY, MULTIDISCIPLINARY | PHOTOREDOX CATALYSIS | Usage | Catalysis | Enantiomers | Aldehydes | Green technology | Solar energy
Journal Article
ChemSusChem, ISSN 1864-5631, 06/2015, Volume 8, Issue 11, pp. 1841 - 1844
Bismuth oxide, an inexpensive and non‐toxic semiconductor, has been successfully used as a visible light photocatalyst for the atom transfer radical addition... 
radical reactions | visible light | bismuth oxide | photocatalysis | addition reactions | ORGANIC-SYNTHESIS | TRANSITION-METAL-COMPLEXES | ORGANOCATALYSIS | POLYMERIZATION | CHEMISTRY, MULTIDISCIPLINARY | PHOTOREDOX CATALYSIS | ALKENES | CHAIN REACTIONS | REDUCING AGENT | PHOTOCHEMISTRY | CYCLIZATION | Olefins | Catalysis
Journal Article
ISSN 1359-7345, 1/2016, Volume 52, Issue 1, pp. 1997 - 21
Recently introduced tris(1,2,3-triazol-4-yl)methanols and derivatives (TTM ligands) have become a valuable subclass of C 3 -symmetric tripodal ligands for... 
Journal Article
Organic Letters, ISSN 1523-7060, 02/2016, Volume 18, Issue 3, pp. 556 - 559
An efficient, highly regio- and stereoselective [4 + 2] cycloaddition reaction to generate tetrahydropyranopyrazole frameworks has been developed. To this end,... 
ACTIVATION | ASYMMETRIC-SYNTHESIS | SPIROPYRAZOLONES |