Cargando…

3-Benzoylisoxazolines by 1,3-Dipolar Cycloaddition: Chloramine-T-Catalyzed Condensation of α-Nitroketones with Dipolarophiles

In this study, 3-benzoylisoxazolines were synthesized by reacting alkenes with various α-nitroketones using chloramine-T as the base. The scope of α-nitroketones and alkenes is extensive, including different alkenes and alkynes to form various isoxazolines and isoxazoles. The use of chloramine-T, as...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pan, Xinhui, Xin, Xiaobing, Mao, Ying, Li, Xin, Zhao, Yanan, Liu, Yidi, Zhang, Ke, Yang, Xiaoda, Wang, Jinhui
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227129/ https://www.ncbi.nlm.nih.gov/pubmed/34201335 http://dx.doi.org/10.3390/molecules26123491

Ejemplares similares

Novel Synthesis of Dihydroisoxazoles by p-TsOH-Participated 1,3-Dipolar Cycloaddition of Dipolarophiles withα-Nitroketones
por: Yang, Caiyun, et al.
Publicado: (2023)

Electron-rich benzofulvenes as effective dipolarophiles in copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides
por: Chang, Xin, et al.
Publicado: (2023)

1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides with Carbonyl Dipolarophiles Yielding Oxazolidine Derivatives
por: Meyer, Adam G., et al.
Publicado: (2016)

Dipolarophile-Controlled Regioselective 1,3-Dipolar Cycloaddition: A Switchable Divergent Access to Functionalized N-Fused Pyrrolidinyl Spirooxindoles
por: Wang, Yongchao, et al.
Publicado: (2023)

Activation of Dinitrogen as A Dipolarophile in 1,3-Dipolar Cycloadditions: A Theoretical Study Using Nitrile Imines as “Octet” 1,3-Dipoles
por: Montero-Campillo, M. Merced, et al.
Publicado: (2017)

An intramolecular relay catalysis strategy for Knoevenagel condensation and 1,3-dipolar cycloaddition domino reactions
por: Yuan, Xiaofeng, et al.
Publicado: (2019)

Nitroacetylene as dipolarophile in [2 + 3] cycloaddition reactions with allenyl-type three-atom components: DFT computational study
por: Jasiński, Radomir
Publicado: (2015)

Understanding the 1,3‐Dipolar Cycloadditions of Allenes
por: Yu, Song, et al.
Publicado: (2020)

Copper(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of 1,3-enynes and azomethine ylides
por: Wang, Bo-Ran, et al.
Publicado: (2023)

Thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition
por: Potratz, Stefanie, et al.
Publicado: (2012)

The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition
por: Breugst, Martin, et al.
Publicado: (2020)

Stereoselective Lewis base catalyzed formal 1,3-dipolar cycloaddition of azomethine imines with mixed anhydrides
por: Hesping, Lena, et al.
Publicado: (2015)

How the Lewis Base F(–) Catalyzes the 1,3-Dipolar Cycloaddition between Carbon Dioxide and Nitrilimines
por: Svatunek, Dennis, et al.
Publicado: (2021)

Cu/TEMPO catalyzed dehydrogenative 1,3-dipolar cycloaddition in the synthesis of spirooxindoles as potential antidiabetic agents
por: Teja, Chitrala, et al.
Publicado: (2020)

Dynamic Catalytic Highly Enantioselective 1,3‐Dipolar Cycloadditions
por: Yildirim, Okan, et al.
Publicado: (2021)

An Overlooked Pathway in 1,3‐Dipolar Cycloadditions of Diazoalkanes with Enamines
por: Li, Le, et al.
Publicado: (2022)

Nitropyridines as 2π-Partners in 1,3-Dipolar Cycloadditions with N-Methyl Azomethine Ylide: An Easy Access to Condensed Pyrrolines
por: Bastrakov, Maxim A., et al.
Publicado: (2021)

Imidazole catalyzes chlorination by unreactive primary chloramines
por: Roemeling, Margo D., et al.
Publicado: (2015)

Triazol-substituted titanocenes by strain-driven 1,3-dipolar cycloadditions
por: Gansäuer, Andreas, et al.
Publicado: (2014)

Green Protocols in Heterocycle Syntheses via 1,3-Dipolar Cycloadditions
por: Martina, Katia, et al.
Publicado: (2019)

Strain-Promoted 1,3-Dipolar Cycloaddition of Cycloalkynes and Organic Azides
por: Dommerholt, Jan, et al.
Publicado: (2016)

Targeted 1,3-dipolar cycloaddition with acrolein for cancer prodrug activation
por: Pradipta, Ambara R., et al.
Publicado: (2021)

The 1,3‐Dipolar Cycloaddition: From Conception to Quantum Chemical Design
por: Beutick, Steven E., et al.
Publicado: (2022)

Mechanistic DFT Study of 1,3-Dipolar Cycloadditions of Azides with Guanidine
por: Antol, Ivana, et al.
Publicado: (2023)

Synthesis of Isoxazole and 1,2,3-Triazole Isoindole Derivatives via Silver- and Copper-Catalyzed 1,3-Dipolar Cycloaddition Reactions †
por: Rammah, Mohamed Mehdi, et al.
Publicado: (2016)

Synthetic scope and DFT analysis of the chiral binap–gold(I) complex-catalyzed 1,3-dipolar cycloaddition of azlactones with alkenes
por: Martín-Rodríguez, María, et al.
Publicado: (2013)

Graphene Oxide Catalyzed Synthesis of Fused Chromeno Spiro Pyrrolidine Oxindoles via Tandem Decarboxylation and 1,3-Dipolar Cycloaddition
por: Singh, Vipin, et al.
Publicado: (2022)

The [3 + 3]-Cycloaddition Alternative for Heterocycle Syntheses: Catalytically Generated Metalloenolcarbenes as Dipolar Adducts
por: Xu, Xinfang, et al.
Publicado: (2014)

Additive-assisted regioselective 1,3-dipolar cycloaddition of azomethine ylides with benzylideneacetone
por: Peng, Chuqin, et al.
Publicado: (2014)

1,3-Dipolar Cycloaddition Reactions of Substituted Benzyl Azides with Acetylenic Compounds
por: Abu-Orabi, Sultan T.
Publicado: (2002)

Decarboxylative 1,3-dipolar cycloaddition of amino acids for the synthesis of heterocyclic compounds
por: Zhang, Xiaofeng, et al.
Publicado: (2023)

Enantioselective 1,3-Dipolar Cycloadditions of α-Methylene Lactams to Construct Spirocycles
por: Nishiura, Yuji, et al.
Publicado: (2023)

1,3-Dipolar cycloaddition of isatin N,N′-cyclic azomethine imines with α,β-unsaturated aldehydes catalyzed by DBU in water
por: Wang, Zhan-Yong, et al.
Publicado: (2020)

Chloramine
Publicado: (1916)

Expanding Stereochemical and Skeletal Diversity Using Petasis Reactions and 1,3-Dipolar Cycloadditions
por: Muncipinto, Giovanni, et al.
Publicado: (2010)

Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Azomethine Ylides for Biology-Oriented Synthesis
por: Narayan, Rishikesh, et al.
Publicado: (2014)

Bioorthogonal prodrug activation driven by a strain-promoted 1,3-dipolar cycloaddition
por: Matikonda, Siddharth S., et al.
Publicado: (2015)

A Diastereoselective Synthesis of Dispiro[oxindole-cyclohexanone]pyrrolidines by 1,3-Dipolar Cycloaddition
por: Anis’kov, Alexander, et al.
Publicado: (2017)

Synthesis of Pyrrolo[2,1-a]isoquinolines by Multicomponent 1,3-Dipolar Cycloaddition
por: Dumitrascu, Florea, et al.
Publicado: (2013)

MOF-Derived Cu@N-C Catalyst for 1,3-Dipolar Cycloaddition Reaction
por: Wang, Zhuangzhuang, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_58k4vt63sp3bm6ckgnd579ftqi