Results 11 to 20 of about 205,200 (319)

Highly enantioselective catalytic synthesis of chiral pyridines

open access: yesNature Communications, 2017
Chiral pyridines are valuable building blocks in medicinal chemistry applications. Here, the authors report the copper-catalysed Lewis acid-assisted asymmetric alkylation of β-substituted alkenyl pyridines with Grignard reagents affording chiral ...
Ravindra P. Jumde   +3 more
doaj   +2 more sources

1H-Pyrazolo[3,4-b]pyridines: Synthesis and Biomedical Applications

open access: yesMolecules, 2022
Pyrazolo[3,4-b]pyridines are a group of heterocyclic compounds presenting two possible tautomeric forms: the 1H- and 2H-isomers. More than 300,000 1H-pyrazolo[3,4-b]pyridines have been described which are included in more than 5500 references (2400 ...
Ana Donaire-Arias   +5 more
semanticscholar   +1 more source

Halogenation of the 3-position of pyridines through Zincke imine intermediates

open access: yesScience, 2022
Pyridine halogenation reactions are crucial for obtaining the vast array of derivatives required for drug and agrochemical development. However, despite more than a century of synthetic endeavors, halogenation processes that selectively functionalize the
Benjamin T. Boyle   +4 more
semanticscholar   +1 more source

Practical and Regioselective Synthesis of C-4-Alkylated Pyridines.

open access: yesJournal of the American Chemical Society, 2021
The direct position-selective C-4 alkylation of pyridines has been a long-standing challenge in heterocyclic chemistry, particularly from pyridine itself.
J. Choi   +3 more
semanticscholar   +1 more source

Recent Advances in the Synthesis of C2‐Functionalized Pyridines and Quinolines Using N ‐Oxide Chemistry

open access: yesAdvanced Synthesis and Catalysis, 2020
. While remarkable progress has recently been made for the direct C-H-functionalization of azines, its application is still limited by a lack of accessible functional groups (primarily carbon-based) and poor regioselectivity.
Dong Wang   +4 more
semanticscholar   +1 more source

2-Sulfonyl pyridines as tunable, cysteine-reactive electrophiles.

open access: yesJournal of the American Chemical Society, 2020
The emerging use of covalent ligands as chemical probes and drugs would benefit from an expanded repertoire of cysteine-reactive electrophiles for efficient and diverse targeting of the proteome.
C. Zambaldo   +14 more
semanticscholar   +1 more source

Fast microwave-assisted oxidation of 1,4-dihydropyridines with FeCl 3.SiO 2 [PDF]

open access: yes, 2005
Pyridine derivatives are easily obtained in high yields by microwave-promoted rapid oxidation of the corresponding 1,4-dihydropyridines with ferric chloride hexahydrate and silica gel under solvent-free ...
Alaee, E.   +4 more
core   +1 more source

Synthesis of Chitosan-La2O3 Nanocomposite and Its Utility as a Powerful Catalyst in the Synthesis of Pyridines and Pyrazoles

open access: yesMolecules, 2021
Recently, the development of nanocatalysts based on naturally occurring polysaccharides has received a lot of attention. Chitosan (CS), as a biodegradable and biocompatible polysaccharide, is considered to be an excellent template for the design of a ...
Khaled D. Khalil   +4 more
doaj   +1 more source

Synthesis and late-stage functionalization of complex molecules through C-H fluorination and nucleophilic aromatic substitution. [PDF]

open access: yes, 2014
We report the late-stage functionalization of multisubstituted pyridines and diazines at the position α to nitrogen. By this process, a series of functional groups and substituents bound to the ring through nitrogen, oxygen, sulfur, or carbon are ...
Fier, Patrick S, Hartwig, John F
core   +3 more sources

4-(Methylamino)pyridine [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2010
The non-H atoms of the title compound, C(6)H(8)N(2), lie in a common plane (r.m.s. deviation = 0.034 Å). In the crystal, adjacent mol-ecules are linked by inter-molecular N-H⋯N hydrogen bonds into a zigzag chain running along the c axis.
openaire   +3 more sources

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