Results 1 to 10 of about 6,970 (213)
Protocol for stereodivergent asymmetric hydrogenation of quinoxalines [PDF]
Summary: Chiral 1,2,3,4-tetrahydroquinoxalines are ubiquitous in natural products and bioactive molecules. Herein, we disclose a protocol for stereodivergent asymmetric hydrogenation of disubstituted quinoxalines for the preparation of both cis- and ...
Mingyang Wang, Chenguang Liu, Qiang Liu
doaj +2 more sources
Benzylic C–H Oxidation: Recent Advances and Applications in Heterocyclic Synthesis [PDF]
Benzylic C–H oxidation to form carbonyl compounds, such as ketones, is a fundamental transformation in organic synthesis as it allows for the preparation of versatile intermediates.
Nonhlelo Majola, Vineet Jeena
doaj +2 more sources
Anticancer, anti-inflammatory and analgesic activities of aminoalcohol-based quinoxaline small molecules [PDF]
Purpose: Bioactive molecules are relevant to fight cancer and associated conditions. Quinoxaline is a privileged N-heterocycle, notably as anticancer agents.
Jannyely Moreira Neri +9 more
doaj +2 more sources
Of the utmost importance of chirality in organic compounds and drugs, the present work reports structure-chirality relationship of three steroidal quinoxalines, which were synthesised by condensing diaminobenzenes with cholestenone.
Rashid Mehmood +4 more
doaj +1 more source
A Green, Scalable, and Catalyst-Free One-Minute Synthesis of Quinoxalines
A highly efficient and catalyst-free protocol is reported for the synthesis of quinoxalines via the classical cyclocondensation reaction between aryldiamines and dicarbonyl compounds.
Vijayaragavan Elumalai, Jørn H. Hansen
doaj +1 more source
: Synthetic N-heterocyclic compounds, such as quinoxalines, have shown a crucial role in pharmaceutical as well as food and dye industries. However, the traditional synthesis toward N-heterocycles relies on multistep energy and cost-intensive non ...
Yu Feng +6 more
doaj +1 more source
4,5-Dihydropyrrolo [1,2-a]quinoxalines are interesting druggable scaffolds, with multifaceted biological properties, including anticancer properties targeting the G protein-coupled estrogen receptor 1 (GPER).
Gabriele Carullo +3 more
doaj +1 more source
A gold-catalyzed protocol to obtain functionalized 3H-pyrrolo [1,2,3-de] quinoxalines from suitable substituted N-alkynyl indoles has been proposed. The mild reaction conditions were revealed to be compatible with different functional groups, including ...
Antonia Iazzetti +5 more
doaj +1 more source
Quinoxaline-2-carbonitrile [PDF]
In the title compound, C9H5N3, the quinoxaline ring is essentially planar, with a maximum deviation of 0.012 (1) Å. Short intermolecular distances between the centroids of the 2,3-dihydropyrazine and benzene rings [3.6490 (5) Å] indicate the existence of π⋯π interactions.
Hoong‐Kun Fun +4 more
openaire +3 more sources
Bis[2-(thiophen-2-yl)quinoxaline-κN4]silver(I) perchlorate
The crystal of the title salt, [Ag(C12H8N2S)2]ClO4, has C2/c symmetry whereby the silver(I) atom sits on a twofold rotation axis, as does the perchlorate anion, which is disordered about this axis.
Guy Crundwell
doaj +1 more source

