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meta-Selective C-H Functionalization of Pyridines.

Angewandte Chemie, 2023
The pyridine moiety is an important core structure for a variety of drugs, agrochemicals, catalysts, and functional materials. Direct functionalization of C-H bonds in pyridines is a straightforward approach to access valuable substituted pyridines ...
Hui Cao, Q. Cheng, A. Studer
semanticscholar   +1 more source

Asymmetric C3-Allylation of Pyridines.

Journal of the American Chemical Society, 2023
Asymmetric intermolecular C-H functionalization of pyridines at C3 is unprecedented. Herein, we report the first examples of such transformations: specifically, C3-allylation of pyridines via tandem borane and iridium catalysis.
Zhong Liu   +6 more
semanticscholar   +1 more source

Radical and ionic meta-C–H functionalization of pyridines, quinolines, and isoquinolines

Science, 2022
Carbon-hydrogen (C−H) functionalization of pyridines is a powerful tool for the rapid construction and derivatization of many agrochemicals, pharmaceuticals, and materials.
Hui Cao, Q. Cheng, A. Studer
semanticscholar   +1 more source

Borane-Catalyzed C3-Alkylation of Pyridines with Imines, Aldehydes, or Ketones as Electrophiles.

Journal of the American Chemical Society, 2022
Achieving C3-selective pyridine functionalization is a longstanding challenge in organic chemistry. The existing methods, including electrophilic aromatic substitution and C-H activation, often require harsh reaction conditions and excess pyridine and ...
Zhong Liu   +7 more
semanticscholar   +1 more source

C3-Selective Trifluoromethylthiolation and Difluoromethylthiolation of Pyridines and Pyridine Drugs via Dihydropyridine Intermediates.

Journal of the American Chemical Society, 2022
Herein, we report a method for unprecedented C3-selective C-H tri- and difluoromethylthiolation of pyridines. The method relies on borane-catalyzed pyridine hydroboration for generation of nucleophilic dihydropyridines; these intermediates react with ...
Xin-Yue Zhou   +4 more
semanticscholar   +1 more source

Visible-Light-Enabled Trifluoromethylative Pyridylation of Alkenes from Pyridines and Triflic Anhydride.

Angewandte Chemie, 2020
A general strategy for visible-light-enabled site-selective trifluoromethylative pyridylation of unactivated alkenes has been developed using pyridines and triflic anhydride (Tf 2 O).
Kangjae Lee   +4 more
semanticscholar   +1 more source

Role of Pyridine in Wyodak−Pyridine Adducts

Energy & Fuels, 2005
When pyridine (PYR) is added to powdered Wyodak subbituminous coal (WYO), the sample is converted to a paste, and the molecular-level adduct which is formed is stable for months. After the excess pyridine has evaporated from the WYO−PYR sample, the stoichiometry of the adduct is ca.
Wertz, David L.   +3 more
openaire   +2 more sources

Recent Developments in Transition-Metal-Free Functionalization and Derivatization Reactions of Pyridines

Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry, 2020
Pyridine is an important structural motif that is prevalent in natural products, drugs, and materials. Methods that functionalize and derivatize pyridines have gained significant attention. Recently, a large number of transition-metal-free reactions have
Fei Zhou, Lei Jiao
semanticscholar   +1 more source

Parallel Interactions at Large Horizontal Displacement in Pyridine–Pyridine and Benzene–Pyridine Dimers

ChemPhysChem, 2012
AbstractA study of crystal structures from the Cambridge Structural Database (CSD) and DFT calculations reveals that parallel pyridine–pyridine and benzene–pyridine interactions at large horizontal displacements (offsets) can be important, similar to parallel benzene–benzene interactions.
Snežana D. Zarić   +3 more
openaire   +4 more sources

Regio- and Enantioselective C-H Cyclization of Pyridines with Alkenes Enabled by a Nickel/N-Heterocyclic Carbene Catalysis.

Journal of the American Chemical Society, 2019
Annulated pyridines are ubiquitous scaffolds in many bioactive molecules. A highly regio- and enantioselective Ni(0)-catalyzed endo-selective C-H cyclization of pyridines with alkenes has been developed.
Wu-Bin Zhang   +4 more
semanticscholar   +1 more source

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