PUBLICACIÓN

Synthesis and immobilisation of 2-aminoimidazole derivatives on the organosilanised surface of Ti6Al4V alloy.

ACCEDER A LA PUBLICACIÓN: Orcid

David Piedrahita, Ignacio López-Coca, María José Arévalo Caballero, Guadalupe SILVERO

2016

DOI

10.3390/ecsoc-20-b017

AUTORES DE LA UEX

María Guadalupe Silvero Enríquez

OTRAS PUBLICACIONES DE INTERÉS

Theoretical Study Of The Facial Selectivity In Diels-Alder Reactions Of 4,4-Disubstituted Cyclohexadienones
Green Heterogeneous Catalysts For Cleaner Solvent-Free Production Of Acetates
The Olive-Tree Leaves As A Source Of High-Added Value Molecules: Oleuropein
Green Heterogeneous Catalysts For Cleaner Solvent-Free Production Of Acetates
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
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Desulfurisation Of Oils Using Ionic Liquids: Selection Of Cationic And Anionic Components To Enhance Extraction Efficiency
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
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
Determination Of Gels Molecular Structure By Computational Calculations
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Determination Of Gels Molecular Structure By Computational Calculations
Theoretical Study Of The Molecular Structure For Zirconium Complexes
Determination Of Gels Molecular Structure By Computational Calculations
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
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
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
Green Heterogeneous Catalysts For Cleaner Solvent-Free Production Of Acetates
WEB ACCESIBLE