Results 61 to 70 of about 12,240 (259)

From Mn(II)3 to Mn(IV)3: Controlled Multielectron Oxidation and Hydrocarbon Oxygenation Within a 7‐Dipy Trinuclear Scaffold

Journal of the Chinese Chemical Society, EarlyView.
A trinuclear manganese complex supported by the 7‐Dipy scaffold undergoes controlled multielectron oxidation from Mn(II)3 to high‐valent Mn(IV)3 states. Spectroscopic signatures, including 16‐line and geff ≈ 5 EPR features, reveal stepwise redox accumulation. The oxidized Mn3 cluster mediates efficient oxygen‐atom transfer to strong CH bonds, enabling
Yu‐Hsuan Chen, Peter Ping‐Yu Chen
wiley   +1 more source

DNA‐Enzyme Hybrid Nanostructures: Functional Materials to Modulate Enzymatic Activity

Small, EarlyView.
DNA–enzyme hybrid nanostructures enable precise spatial and stoichiometric control over enzyme organization, offering a powerful platform to modulate catalytic activity. This review critically evaluates key mechanistic hypotheses, including proximity effects, microenvironment changes, confinement, and stabilization, as well as highlighting ...
Manar Elnaggar, Amelie Heuer‐Jungemann
wiley   +1 more source

Synthesis of Sterically Shielded Nitroxides Using the Reaction of Nitrones with Alkynylmagnesium Bromides

Molecules, 2022
Sterically shielded nitroxides, which demonstrate high resistance to bioreduction, are the spin labels of choice for structural studies inside living cells using pulsed EPR and functional MRI and EPRI in vivo.
Sergey A. Dobrynin, Mark M. Gulman, Denis A. Morozov, Irina F. Zhurko, Andrey I. Taratayko, Yulia S. Sotnikova, Yurii I. Glazachev, Yuri V. Gatilov, Igor A. Kirilyuk   +8 more
doaj   +1 more source

Synthesis of 2‐Aza‐Bicyclo[4.3.0]nonane Derivatives Related to the Camporidines via Intramolecular [3+2]‐Cycloaddition

European Journal of Organic Chemistry, Volume 29, Issue 24, 23 June 2026.
The intramolecular nitrile oxide olefin [3 + 2]‐cycloaddition offers a reliable entry toward 2‐aza‐bicyclo[4.3.0]‐nonanes, a substructure found in several bioactive piperidine alkaloids. The required oxime precursors were prepared in non‐racemic form by Ir‐catalyzed asymmetric allylation and ring‐closing metathesis.
Alicia Köcher, Tobias Wilczek, Nora Katharina Korber, Jörg-Martin Neudörfl, Bernd Goldfuss, Hans-Günther Schmalz   +5 more
wiley   +1 more source

1,1‐Disubstituted Vinylbromides: Versatile Building Blocks for the Synthesis of Nitrogen‐Containing Heterocycles

European Journal of Organic Chemistry, Volume 29, Issue 23, 16 June 2026.
1,1‐Disubstituted vinylbromides are key intermediates for constructing nitrogen‐containing heterocycles. This review provides an overview of the synthetic applications of 1,1‐disubstituted vinylbromides and summarizes recent developments in reaction methodologies, mechanistic insights, and the structural diversity of N‐heterocyclic compounds accessible
Anne Westermeyer, Jun Fang, Chonghuo Liu, Guillaume Lefèvre, Gérard Guillamot, Phannarath Phansavath, Virginie Ratovelomanana‐Vidal   +6 more
wiley   +1 more source

Highly Electron-Deficient Pyridinium-Nitrones for Rapid and Tunable Inverse-Electron-Demand Strain-Promoted Alkyne-Nitrone Cycloaddition.

Organic Letters, 2019
Highly accelerated inverse-electron-demand strain-promoted alkyne-nitrone cycloaddition (IED SPANC) between a stable cyclooctyne (bicyclo[6.1.0]nonyne (BCN)) and nitrones delocalized into a C α-pyridinium functionality is reported, with the most electron-
Praveen N. Gunawardene, Wilson Luo, Alexander M. Polgar, J. Corrigan, M. Workentin   +4 more
semanticscholar   +1 more source

Electrophilic Iodination of Heterocyclic Compounds. Recent Advances 2008–2025: Part II

European Journal of Organic Chemistry, Volume 29, Issue 22, 9 June 2026.
Electrophilic iodination using molecular iodine and iodide sources represents an efficient approach for accessing valuable iodinated organic compounds. This review highlights recent advances in the iodination of heterocyclic compounds from 2008 to 2025, emphasizing the role of heteroaryl iodides as important synthetic intermediates for biologically ...
Njomza Ajvazi, Stojan Stavber
wiley   +1 more source

STUDY OF CYCLOREVERSION OF NTTRONE-CY CLODIMERS [PDF]

Journal of Sciences, Islamic Republic of Iran, 1993
A series of 1,3-dipolar cycloaddition reactions are carried out using cyclodimers of simple nitrones and various dipolarophiles; substituted isoxazolidines are isolated and identified.
doaj  

Lighting the Path to Cyclic Phosphonamides via Halogen‐Bond Electron Donor–Acceptor Activation

Advanced Synthesis &Catalysis, Volume 368, Issue 11, 3 June 2026.
Cyclic phosphinamides are valuable scaffolds for optoelectronic applications, yet remain difficult to access with existing methods. Here, we highlight a mild and straightforward visible light‐driven strategy that enables the formation of cyclic phosphinamides and thiophosphinamides.
Clara Faure, Yurong Yuan, Diana Lamaa, Thomas Gaslonde, Etienne Derat, Sonia Lajnef, Fabienne Peyrot, Philippe Belmont, Etienne Brachet   +8 more
wiley   +1 more source

Dialkylzinc-Assisted Alkynylation of Nitrones

, 2002
International audienceReaction of nitrones with terminal alkynes takes place readily in the presence of a substoichiometric amt.
Chavant, Pierre Yves, Urvish Pandya, Shashi, Ayling, Alexander, Pinet, Sandra, Vallée, Yannick   +4 more
core   +1 more source