Results 141 to 150 of about 110,104 (297)

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

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
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   +6 more
wiley   +1 more source

Emerging Trends in Organic Photoreactions Utilizing Disulfides

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Disulfides are versatile, nontoxic alternatives to metal photocatalysts. This review explores their role as photoactivated thiyl‐radical precursors and bifunctional catalysts (HAT/electron shuttling) in diverse transformations. Strategies for electronic tuning and development into recyclable heterogeneous materials are highlighted for sustainable ...
Sunil Kumar   +3 more
wiley   +1 more source

Analysis of cyclohexane, cyclopentane, and benzene conformations in ligands for PDB X-ray structures using the Hill-Reilly approach. [PDF]

open access: yesJ Cheminform
Bučeková G   +8 more
europepmc   +1 more source

Photochemical Decatungstate‐Catalyzed Hydroacylation of Maleimides

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
A photocatalytic protocol to access substituted succinimides via tetra‐n‐butylammonium decatungstate photocatalysis is reported. This direct radical‐driven hydroacylation of a variety of N‐substituted maleimides shows tolerance to various aldehydes (or alkanes), affording differentially substituted succinimides in high yields. Succinimides constitute a
Manos V. G. Lantzanakis   +2 more
wiley   +1 more source

Methane Catalytic Amidation via a Plausible Copper-Nitrene Intermediate. [PDF]

open access: yesJ Am Chem Soc
Martínez-Laguna J   +6 more
europepmc   +1 more source

1,2,6‐Thiadiazin‐4‐ones: Robust Photocatalysts for the Green Aerobic Oxidation of Sulfides to Sulfoxides

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
A new photocatalyst for the aerobic photochemical oxidation of sulfides to sulfoxides is described under really low catalyst loading (0.01 mol%) and methanol as the green solvent. The chemoselective oxidation of sulfides to sulfoxides is accomplished using a new family of photocatalysts, namely 1,2,6‐thiadiazin‐4‐ones. Utilizing a low catalyst loading (
Charikleia I. Karaousta   +6 more
wiley   +1 more source

Porcine Liver Esterase‐Catalyzed Dynamic Kinetic Resolution of a Lactone‐Bridged Biaryl: Impact of Organic Cosolvents on Enantioselectivity

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
A stereolabile lactone‐bridged biaryl enables dynamic kinetic resolution to provide a conformationally stable ring‐opened biaryl. A significant positive effect of water‐immiscible organic cosolvents on the enantioselectivity in a reaction catalyzed by porcine liver esterase has been discovered for the first time.
Neha Dhiman   +6 more
wiley   +1 more source

New Insights into Intersystem Crossing in Substituted Aromatics: Singlet-Triplet Conversion in Carbonyl-Substituted Anthracenes. [PDF]

open access: yesJ Phys Chem B
Guarin CA   +6 more
europepmc   +1 more source

Unlocking the Functionalization and Reactivity of Ethylene Bridges in [2.2]Paracyclophanes: Strategies and Challenges

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Bridging the gap. Beyond deck functionalization, the ethylene bridges of [2.2]paracyclophanes offer a largely unexploited reactivity landscape. This review showcases strategies to functionalize these bridges and leverage them to build novel cyclophane architectures.
Rongyu Sun   +3 more
wiley   +1 more source

Silver-Based Alcohol-Functionalized Solvent for Efficient Separation of Olefins. [PDF]

open access: yesChem Bio Eng
Kang H   +8 more
europepmc   +1 more source

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