Cargando…

Growth of Fullerene Fragments Using the Diels-Alder Cycloaddition Reaction: First Step towards a C(60) Synthesis by Dimerization

Density Functional Theory has been used to model the Diels-Alder reactions of the fullerene fragments triindenetriphenilene and pentacyclopentacorannulene with ethylene and 1,3-butadiene. The purpose is to prove the feasibility of using Diels-Alder cycloaddition reactions to grow fullerene fragments...

Descripción completa

Detalles Bibliográficos
Autores principales:	Mojica, Martha, Méndez, Francisco, Alonso, Julio A.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2013
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270520/ https://www.ncbi.nlm.nih.gov/pubmed/23434874 http://dx.doi.org/10.3390/molecules18022243

Ejemplares similares

The Diels-Alder Cycloaddition Reaction of Substituted Hemifullerenes with 1,3-Butadiene: Effect of Electron-Donating and Electron-Withdrawing Substituents
por: Mojica, Martha, et al.
Publicado: (2016)

Synthesis and Diels–Alder cycloaddition reaction of norbornadiene and benzonorbornadiene dimers
por: Nişancı, Bilal, et al.
Publicado: (2009)

Diels–Alder Cycloaddition Reactions in Sustainable Media
por: Soares, Maria I. L., et al.
Publicado: (2022)

On the regioselectivity of the Diels–Alder cycloaddition to C(60) in high spin states
por: El Bakouri, Ouissam, et al.
Publicado: (2018)

Successive Diels–Alder Cycloadditions of Cyclopentadiene to [10]CPP⊃C(60): A Computational Study
por: Pareras, Gerard, et al.
Publicado: (2022)

Reversible Diels–Alder Addition to Fullerenes: A Study of Dimethylanthracene with H(2)@C(60)
por: Subhani, Mahboob, et al.
Publicado: (2022)

Effect of substituents and promoters on the Diels–Alder cycloaddition reaction in the biorenewable synthesis of trimellitic acid
por: Khan, Tuhin Suvra, et al.
Publicado: (2020)

Hetero‐Diels–Alder Cycloaddition with RAFT Polymers as Bioconjugation Platform
por: Beloqui, Ana, et al.
Publicado: (2020)

Synthesis of the [11]Cyclacene Framework by Repetitive Diels–Alder Cycloadditions
por: Bauer, John B., et al.
Publicado: (2021)

η(6)‐Metalated Aryl Iodides in Diels‐Alder Cycloaddition Reactions: Mode of Activation and Catalysis
por: Portela, Susana, et al.
Publicado: (2022)

The hexadehydro-Diels–Alder reaction
por: Hoye, Thomas R., et al.
Publicado: (2012)

The pentadehydro-Diels–Alder reaction
por: Wang, Teng, et al.
Publicado: (2016)

An on‐surface Diels–Alder reaction
por: Castro‐Esteban, Jesús, et al.
Publicado: (2021)

Diels-Alder cycloadditions in water for the straightforward preparation of peptide–oligonucleotide conjugates
por: Marchán, Vicente, et al.
Publicado: (2006)

Diels-Alder cycloadditions in water for the straightforward preparation of peptide–oligonucleotide conjugates
por: Marcha´n, Vicente, et al.
Publicado: (2006)

Secondary Orbital Interactions Enhance the Reactivity of Alkynes in Diels–Alder Cycloadditions
por: Levandowski, Brian J., et al.
Publicado: (2019)

Silylium ion mediated 2+2 cycloaddition leads to 4+2 Diels-Alder reaction products
por: Wang, Heng-Ding, et al.
Publicado: (2020)

Electronic Structure Analysis of the Diels–Alder Cycloaddition Catalyzed by Alkali-Exchanged Faujasites
por: Rohling, Roderigh Y., et al.
Publicado: (2018)

Correction to “Secondary Orbital Interactions Enhance the Reactivity of Alkynes in Diels–Alder Cycloadditions”
por: Levandowski, Brian J., et al.
Publicado: (2019)

Origin of asynchronicity in Diels–Alder reactions
por: Vermeeren, Pascal, et al.
Publicado: (2021)

Synthesis of mixed musks via Eschenmoser–Tanabe fragmentation, enyne metathesis and Diels–Alder reaction as key steps
por: Kotha, Sambasivarao, et al.
Publicado: (2022)

Highly Regio- and Stereoselective Diels-Alder Cycloadditions via Two-Step and Multicomponent Reactions Promoted by Infrared Irradiation under Solvent-Free Conditions
por: Flores-Conde, Maria Ines, et al.
Publicado: (2012)

Functionalization of Single-Walled Carbon Nanotubes with End-Capped Polystyrene via a Single-Step Diels–Alder Cycloaddition
por: Stathouraki, Maria-Malvina, et al.
Publicado: (2021)

Diels–Alder reactions in confined spaces: the influence of catalyst structure and the nature of active sites for the retro-Diels–Alder reaction
por: Cantín, Ángel, et al.
Publicado: (2016)

Diels–Alder cycloadditions of N-arylpyrroles via aryne intermediates using diaryliodonium salts
por: Chen, Huangguan, et al.
Publicado: (2018)

[2 + 1] Cycloaddition reactions of fullerene C(60) based on diazo compounds
por: Biglova, Yuliya N
Publicado: (2021)

Molecular design principles towards exo-exclusive Diels–Alder reactions
por: Huang, Ci-Jhang, et al.
Publicado: (2019)

Dual Activation of Aromatic Diels–Alder Reactions
por: Narsaria, Ayush K., et al.
Publicado: (2019)

Diels–Alder Reactions During the Biosynthesis of Sorbicillinoids
por: Kahlert, Lukas, et al.
Publicado: (2020)

The simplest Diels–Alder reactions are not endo-selective
por: Lording, William J., et al.
Publicado: (2020)

How Ionization Catalyzes Diels‐Alder Reactions
por: Vermeeren, Pascal, et al.
Publicado: (2022)

How Bases Catalyze Diels‐Alder Reactions
por: Yu, Song, et al.
Publicado: (2022)

Exploiting Double Exchange Diels-Alder Cycloadditions for Immobilization of Peptide Nucleic Acids on Gold Nanoparticles
por: Cadoni, Enrico, et al.
Publicado: (2020)

Elucidation of the stereocontrol mechanisms of the chemical and biosynthetic intramolecular Diels–Alder cycloaddition for the formation of bioactive decalins
por: Kariya, Takumi, et al.
Publicado: (2023)

The [4+2]‐Cycloaddition of α‐Nitrosoalkenes with Thiochalcones as a Prototype of Periselective Hetero‐Diels–Alder Reactions—Experimental and Computational Studies
por: Mlostoń, Grzegorz, et al.
Publicado: (2019)

Intermolecular Diels-Alder Cycloadditions of Furfural-Based Chemicals from Renewable Resources: A Focus on the Regio- and Diastereoselectivity in the Reaction with Alkenes
por: Galkin, Konstantin I., et al.
Publicado: (2021)

High stereoselectivity on low temperature Diels-Alder reactions
por: da Silva Filho, Luiz Carlos, et al.
Publicado: (2005)

How Lewis Acids Catalyze Diels–Alder Reactions
por: Vermeeren, Pascal, et al.
Publicado: (2020)

Cross-Linking of Polypropylene via the Diels–Alder Reaction
por: Muljana, Henky, et al.
Publicado: (2022)

Radical cation Diels–Alder reactions of arylidene cycloalkanes
por: Nakayama, Kaii, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_brk69poav4o0sijeooso6b41q8