PUBLICACIÓN

The olive-tree leaves as a source of high-added value molecules: Oleuropein

ACCEDER A LA PUBLICACIÓN: Scopus

2020 Studies in Natural Products Chemistry

CITAS

51

DOI

10.1016/b978-0-12-817903-1.00005-x

EID

2-s2.0-85079434047

ISSN

1572-5995

AUTORES DE LA UEX

María Guadalupe Silvero Enríquez
Ignacio López-Coca Martín

OTRAS PUBLICACIONES DE INTERÉS

Reactions Of Thioamides With Metal Carboxylates In Organic Media
Manual De Evaluación De La Calidad Del Agua En Charcas Ganaderas
Exploring A Water–ethyl Acetate System For The Efficient Synthesis Of 4-Aryl Quinolines
Manual De Evaluación De La Calidad Del Agua En Charcas Ganaderas
Exploring A Water–ethyl Acetate System For The Efficient Synthesis Of 4-Aryl Quinolines
Catalytic Innovations In The Aza-Michael Reaction: An Experimental Benchmarking Focused On Sustainable Approaches
Exploring A Water–ethyl Acetate System For The Efficient Synthesis Of 4-Aryl Quinolines
Catalytic Innovations In The Aza-Michael Reaction: An Experimental Benchmarking Focused On Sustainable Approaches
Green And One-Pot Synthesis Of 2-Amino-3-Cyanopyridines And Ortho-Aminocarbonitriles As Valuable Biological Compounds Catalyzed By Fe3o4/sio2/ppa As A Magnetic Nanocatalyst
Catalytic Innovations In The Aza-Michael Reaction: An Experimental Benchmarking Focused On Sustainable Approaches
Green And One-Pot Synthesis Of 2-Amino-3-Cyanopyridines And Ortho-Aminocarbonitriles As Valuable Biological Compounds Catalyzed By Fe3o4/sio2/ppa As A Magnetic Nanocatalyst
Bionanocomposites Preparation By Design: Planning Based On The Modification Of Ceria Nanoparticles By Polydopamine Interleaved With The Chitosan Biopolymer
Green And One-Pot Synthesis Of 2-Amino-3-Cyanopyridines And Ortho-Aminocarbonitriles As Valuable Biological Compounds Catalyzed By Fe3o4/sio2/ppa As A Magnetic Nanocatalyst
Bionanocomposites Preparation By Design: Planning Based On The Modification Of Ceria Nanoparticles By Polydopamine Interleaved With The Chitosan Biopolymer
A Fluorescent Furan-Based Probe With Protected Functional Groups For Highly Selective And Non-Toxic Imaging Of Ht-29 Cancer Cells And 4t1 Tumors
Bionanocomposites Preparation By Design: Planning Based On The Modification Of Ceria Nanoparticles By Polydopamine Interleaved With The Chitosan Biopolymer
A Fluorescent Furan-Based Probe With Protected Functional Groups For Highly Selective And Non-Toxic Imaging Of Ht-29 Cancer Cells And 4t1 Tumors
Reinvigorating Aza-Michael Reactions Under Ionic Liquid Catalysis: A Greener Approach†
A Fluorescent Furan-Based Probe With Protected Functional Groups For Highly Selective And Non-Toxic Imaging Of Ht-29 Cancer Cells And 4t1 Tumors
Reinvigorating Aza-Michael Reactions Under Ionic Liquid Catalysis: A Greener Approach†
Ring Opening Polymerization Used For The Production Of Voc Free High-Performance Ecofriendly Novel Pbz/pda/ceo2 Nanocomposites
Reinvigorating Aza-Michael Reactions Under Ionic Liquid Catalysis: A Greener Approach†
Ring Opening Polymerization Used For The Production Of Voc Free High-Performance Ecofriendly Novel Pbz/pda/ceo2 Nanocomposites
Green Heterogeneous Catalysts For Cleaner Solvent-Free Production Of Acetates
Ring Opening Polymerization Used For The Production Of Voc Free High-Performance Ecofriendly Novel Pbz/pda/ceo2 Nanocomposites
Green Heterogeneous Catalysts For Cleaner Solvent-Free Production Of Acetates
From Waste To Resource: Utilizing Sweet Chestnut Waste To Produce Hydrothermal Carbon For Water Decontamination
Green Heterogeneous Catalysts For Cleaner Solvent-Free Production Of Acetates
From Waste To Resource: Utilizing Sweet Chestnut Waste To Produce Hydrothermal Carbon For Water Decontamination
Use Of Phosphorylated Chitosan/alumina Nanoadditives For Polymer Performance Improvement
From Waste To Resource: Utilizing Sweet Chestnut Waste To Produce Hydrothermal Carbon For Water Decontamination
Use Of Phosphorylated Chitosan/alumina Nanoadditives For Polymer Performance Improvement
Solvatochromism Study Of Donor–acceptor Blue Fluorophore And Its Application In Cation And Oxidant Sensing
Use Of Phosphorylated Chitosan/alumina Nanoadditives For Polymer Performance Improvement
Solvatochromism Study Of Donor–acceptor Blue Fluorophore And Its Application In Cation And Oxidant Sensing
Carbon–heteroatom Bond Formation Via Coupling Reactions Performed On A Magnetic Nanoparticle Bed
Solvatochromism Study Of Donor–acceptor Blue Fluorophore And Its Application In Cation And Oxidant Sensing
Carbon–heteroatom Bond Formation Via Coupling Reactions Performed On A Magnetic Nanoparticle Bed
The Olive-Tree Leaves As A Source Of High-Added Value Molecules: Oleuropein
Carbon–heteroatom Bond Formation Via Coupling Reactions Performed On A Magnetic Nanoparticle Bed
The Olive-Tree Leaves As A Source Of High-Added Value Molecules: Oleuropein
Synthesis And Immobilisation Of 2-Aminoimidazole Derivatives On The Organosilanised Surface Of Ti6al4v Alloy.
The Olive-Tree Leaves As A Source Of High-Added Value Molecules: Oleuropein
Synthesis And Immobilisation Of 2-Aminoimidazole Derivatives On The Organosilanised Surface Of Ti6al4v Alloy.
Ionic Liquids: Opportunities For Science And Technology: Overview And Highlights
Synthesis And Immobilisation Of 2-Aminoimidazole Derivatives On The Organosilanised Surface Of Ti6al4v Alloy.
Ionic Liquids: Opportunities For Science And Technology: Overview And Highlights
A Bioinspired Look At The Glucosinolate Metabolic Pathway. Structural Insights Into The Reaction Of Benzyl Isothiocyanate And D-Glucosamine
Ionic Liquids: Opportunities For Science And Technology: Overview And Highlights
A Bioinspired Look At The Glucosinolate Metabolic Pathway. Structural Insights Into The Reaction Of Benzyl Isothiocyanate And D-Glucosamine
Task-Oriented Use Of Ionic Liquids: Efficient Acetylation Of Alcohols And Phenols
A Bioinspired Look At The Glucosinolate Metabolic Pathway. Structural Insights Into The Reaction Of Benzyl Isothiocyanate And D-Glucosamine
Task-Oriented Use Of Ionic Liquids: Efficient Acetylation Of Alcohols And Phenols
Azodicarhoxamides Vs. Azodicarboxylates In Reactions Against Thioisomünchnones: 1,3-Dipolar Cycloaddition Or Nucleophilic Addition?
Task-Oriented Use Of Ionic Liquids: Efficient Acetylation Of Alcohols And Phenols
Azodicarhoxamides Vs. Azodicarboxylates In Reactions Against Thioisomünchnones: 1,3-Dipolar Cycloaddition Or Nucleophilic Addition?
Facile Synthesis Of 4,5-Dihydro-1,3,4-Thiadiazoles By 1,3-Dipolar Cycloaddition Of Thioisomünchnones
Azodicarhoxamides Vs. Azodicarboxylates In Reactions Against Thioisomünchnones: 1,3-Dipolar Cycloaddition Or Nucleophilic Addition?
Facile Synthesis Of 4,5-Dihydro-1,3,4-Thiadiazoles By 1,3-Dipolar Cycloaddition Of Thioisomünchnones
Desulfurisation Of Oils Using Ionic Liquids: Selection Of Cationic And Anionic Components To Enhance Extraction Efficiency
Facile Synthesis Of 4,5-Dihydro-1,3,4-Thiadiazoles By 1,3-Dipolar Cycloaddition Of Thioisomünchnones
Desulfurisation Of Oils Using Ionic Liquids: Selection Of Cationic And Anionic Components To Enhance Extraction Efficiency
Optimising An Artificial Neural Network For Predicting The Melting Point Of Ionic Liquids
Desulfurisation Of Oils Using Ionic Liquids: Selection Of Cationic And Anionic Components To Enhance Extraction Efficiency
Optimising An Artificial Neural Network For Predicting The Melting Point Of Ionic Liquids
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Optimising An Artificial Neural Network For Predicting The Melting Point Of Ionic Liquids
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Anion And Cation Effects On Imidazolium Salt Melting Points: A Descriptor Modelling Study
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Anion And Cation Effects On Imidazolium Salt Melting Points: A Descriptor Modelling Study
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Anion And Cation Effects On Imidazolium Salt Melting Points: A Descriptor Modelling Study
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Determination Of Gels Molecular Structure By Computational Calculations
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Determination Of Gels Molecular Structure By Computational Calculations
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Determination Of Gels Molecular Structure By Computational Calculations
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Theoretical Study Of The Molecular Structure For Zirconium Complexes
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Theoretical Study Of The Molecular Structure For Zirconium Complexes
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
Theoretical Study Of The Molecular Structure For Zirconium Complexes
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone-Alkene Cycloaddition Reaction
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone-Alkene Cycloaddition Reaction
Erratum: Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone - Alkene Cycloaddition Reaction (European Journal Of Organic Chemistry (2001) (2135-2144))
Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone-Alkene Cycloaddition Reaction
Erratum: Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone - Alkene Cycloaddition Reaction (European Journal Of Organic Chemistry (2001) (2135-2144))
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
Erratum: Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone - Alkene Cycloaddition Reaction (European Journal Of Organic Chemistry (2001) (2135-2144))
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Theoretical Study Of The Facial Selectivity In Diels-Alder Reactions Of 4,4-Disubstituted Cyclohexadienones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Theoretical Study Of The Facial Selectivity In Diels-Alder Reactions Of 4,4-Disubstituted Cyclohexadienones
Importancia De Los Compuestos Fenólicos En Los Vinos
Theoretical Study Of The Facial Selectivity In Diels-Alder Reactions Of 4,4-Disubstituted Cyclohexadienones
Importancia De Los Compuestos Fenólicos En Los Vinos
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Importancia De Los Compuestos Fenólicos En Los Vinos
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Manual De Evaluación De La Calidad Del Agua En Charcas Ganaderas
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