Results 71 to 80 of about 9,595 (171)

rac-(2R,3S)-2-Phenyl-3-(3-phenyl-1,2,3,4-tetrahydroquinoxalin-2-yl)quinoxaline

open access: yesActa Crystallographica Section E, 2008
The title compound, C28H22N4, is the unexpected by-product of the reaction of 2-hydroxyacetophenone and 1,2-diaminobenzene under iodine catalysis, during which a carbon–carbon σ-bond between two quinoxaline units was formed.
Sven Ammermann   +4 more
doaj   +1 more source

Edible Qualities and Flavor Omics of Peanut‐Soybean Dajiang

open access: yesFood Science &Nutrition, Volume 14, Issue 3, March 2026.
Dajiang is a fermented beans‐based condiment that is widely popular in Northeast China. In this study, peanut‐soybean Dajiang was successfully prepared by adding peanut to the Dajiang production process and optimizing the fermentation conditions. It was found that the addition of peanuts significantly enhanced the umami, saltiness and compound taste of
Yu Miao   +5 more
wiley   +1 more source

Biotrophic Interactions Between a Mycoparasitic Ampelomyces Fungus and Podosphaera xanthii on Fungicide‐Treated Melon Leaves

open access: yesPlant Pathology, Volume 75, Issue 2, March/April 2026.
The digital micrographs show images of the infection progress by the mycoparasitic Ampelomyces strain in a melon powdery mildew fungus Podosphaera xanthii that was treated with kresoxim‐methyl and sprayed with Ampelomyces spores under the high‐humidity conditions of a growth chamber.
Yuito Sato   +6 more
wiley   +1 more source

One-pot three-component synthesis of quinoxaline and phenazine ring systems using Fischer carbene complexes

open access: yesBeilstein Journal of Organic Chemistry, 2010
One-pot three-component coupling of o-alkynylheteroaryl carbonyl derivatives with Fischer carbene complexes and dienophiles leading to the synthesis of quinoxaline and phenazine ring systems has been investigated. This involves the generation of furo[3,4-
Priyabrata Roy, Binay Krishna Ghorai
doaj   +1 more source

SYNTHESIS OF QUINOXALINES

open access: yes, 2023
Quinoxalines are a group of antibiotics widely used in medicine to fight bacterial infections.These antibiotics have a broad spectrum of action and belong to the class of 4 quinolones. Theirmechanism of action is based on inhibiting the activity of bacterial enzymes responsible for DNAsynthesis, which leads to their death. Due to this, quinoxalines are
openaire   +1 more source

Crystal structure and Hirshfeld surface analysis of 3-phenyl-1-{3-[(3-phenylquinoxalin-2-yl)oxy]propyl}-1,2-dihydroquinoxalin-2-one

open access: yesActa Crystallographica Section E: Crystallographic Communications
In the title compound, C31H24N4O2, the quinoxaline units are distinctly non-planar and twisted end-to-end. In the crystal, C—H...O and C—H...N hydrogen bonds link the molecules into chains extending along the a-axis direction.
Nadeem Abad   +5 more
doaj   +1 more source

Ethyl 2-(3-oxo-1,2,3,4-tetrahydroquinoxalin-2-yl)acetate

open access: yesIUCrData, 2018
In the title compound, C12H14N2O3, the conformation of the ester substituent is partially determined by an intramolecular N—H...O hydrogen bond. The crystal packing consists of layers parallel to (\overline{1}12) held together by N—H...O and C—H...O ...
Nadeem Abad   +5 more
doaj   +1 more source

2-Phenylthieno[2,3-b]quinoxaline

open access: yesActa Crystallographica Section E Structure Reports Online, 2012
The title compound, C(16)H(10)N(2)S, is almost planar (r.m.s. deviation for all non-H atoms = 0.080 Å). The dihedral angle between the three fused-ring system and the phenyl ring is 9.26 (3)°. The S atom and the opposite C atom of the thio-phene ring are mutually disordered with an occupancy ratio of 0.7706 (19):0.2294 (19).
Youssef Ramli   +4 more
openaire   +3 more sources

Chemistry and pharmacological diversity of quinoxaline motifs as anticancer agents

open access: yesActa Pharmaceutica, 2019
Surpassing heart diseases, cancer is taking the lead as the deadliest disease because of its fast rate of spreading in all parts of the world. Tireless commitment to searching for novel therapeutic medicines is a worthwhile adventure in synthetic ...
Ajani Olayinka O.   +5 more
doaj   +1 more source

Ionic liquid 1-butyl-3-methylimidazolium bromide ([bmim]Br): a green and neutral reaction media for the efficient, catalyst-free synthesis of quinoxaline derivatives [PDF]

open access: yesJournal of the Serbian Chemical Society, 2010
Quinoxaline derivatives were produced in excellent yields and short reaction times via the condensation of 1,2-diamines with 1,2-diketones in the neutral ionic liquid 1-butyl-3-methylimidazolium bromide ([bmim]Br) under catalyst-free and microwave ...
MAASOOMEH KHEDRI   +9 more
doaj  

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