Cargando…

Diels–Alder Cycloaddition with CO, CO(2), SO(2), or N(2) Extrusion: A Powerful Tool for Material Chemistry

Phenyl, naphthyl, polyarylphenyl, coronene, and other aromatic and polyaromatic moieties primarily influence the final materials’ properties. One of the synthetic tools used to implement (hetero)aromatic moieties into final structures is Diels–Alder cycloaddition (DAC), typically combined with Schol...

Descripción completa

Detalles Bibliográficos
Autores principales:	Krompiec, Stanisław, Kurpanik-Wójcik, Aneta, Matussek, Marek, Gołek, Bogumiła, Mieszczanin, Angelika, Fijołek, Aleksandra
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745824/ https://www.ncbi.nlm.nih.gov/pubmed/35009318 http://dx.doi.org/10.3390/ma15010172

Ejemplares similares

Nitrile Oxide, Alkenes, Dipolar Cycloaddition, Isomerization and Metathesis Involved in the Syntheses of 2-Isoxazolines
por: Krompiec, Stanisław, et al.
Publicado: (2023)

Diels–Alder Cycloaddition to the Bay Region of Perylene and Its Derivatives as an Attractive Strategy for PAH Core Expansion: Theoretical and Practical Aspects
por: Kurpanik, Aneta, et al.
Publicado: (2020)

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

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

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)

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

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)

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

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

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)

Diastereo‐ and Enantioselective Inverse‐Electron‐Demand Diels–Alder Cycloaddition between 2‐Pyrones and Acyclic Enol Ethers
por: Huang, Guanghao, et al.
Publicado: (2022)

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

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)

Ruthenium-Catalyzed [2 + 2] versus Homo Diels–Alder [2 + 2 + 2] Cycloadditions of Norbornadiene and Disubstituted Alkynes: A DFT Study
por: Pounder, Austin, et al.
Publicado: (2020)

Mechanistic Insight into the [4 + 2] Diels–Alder Cycloaddition over First Row d-Block Cation-Exchanged Faujasites
por: Rohling, Roderigh Y., et al.
Publicado: (2018)

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

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

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

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)

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)

Total Synthesis of Ophiorrhine A, G and Ophiorrhiside E Featuring a Bioinspired Intramolecular Diels–Alder Cycloaddition
por: Cao, Wei, et al.
Publicado: (2022)

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

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)

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)

Efficient synthesis of fully renewable, furfural-derived building blocks via formal Diels–Alder cycloaddition of atypical addends
por: Cioc, Răzvan C., et al.
Publicado: (2023)

A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines†
por: Branowska, Danuta
Publicado: (2005)

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)

Growth of Fullerene Fragments Using the Diels-Alder Cycloaddition Reaction: First Step towards a C(60) Synthesis by Dimerization
por: Mojica, Martha, et al.
Publicado: (2013)

Selective Modification of Ribosomally Synthesized and Post‐Translationally Modified Peptides (RiPPs) through Diels–Alder Cycloadditions on Dehydroalanine Residues
por: de Vries, Reinder H., 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)

An Active Alkali-Exchanged Faujasite Catalyst for p-Xylene Production via the One-Pot Diels–Alder Cycloaddition/Dehydration Reaction of 2,5-Dimethylfuran with Ethylene
por: Rohling, Roderigh Y., et al.
Publicado: (2017)

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)

Cannot write session to /tmp/vufind_sessions/sess_tjeuco8oh41ui4tgrb76ft359k