Results 41 to 50 of about 1,770 (208)
Copper-Mediated Decarboxylative C–H Arylation of Phenol Derivatives with ortho-Nitrobenzoic Acids Using Phenanthroline-Based Bidentate Auxiliary [PDF]
A copper-mediated decarboxylative C–H arylation of phenol derivatives with ortho-nitrobenzoic acid salts via phenanthroline-directed C–H cleavage has been developed.
Hayashi, Yoshihiro +4 more
core +1 more source
Morpholinium 5-chloro-2-nitrobenzoate
In the title compound, C4H10NO+·C7H3ClNO4−, two cations and two anions are connected by N—H⋯O hydrogen bonds to afford a ring with descriptor R44(12), which is located on an inversion center. There are four C—H⋯O interactions which connect the ring units to form a three-dimensional network.
Hiroyuki Ishida +2 more
openaire +1 more source
Our study suggests that Opuntia ficus indica cladode juice exhibits hepatoprotective properties, mitigating liver damage induced by nickel exposure. The polyphenol content was determined using spectrophotometric analysis and HPLC‐MS. Experimental hepatotoxicity was induced by intraperitoneal (i.p.) injection of NiSO4.
Sara Razzak +13 more
wiley +1 more source
2,4,6-Trimethylpyridinium 4-nitrobenzoate–4-nitrobenzoic acid (1/1)
The asymmetric unit of the title co-crystal, C8H12N+·C7H4NO4−·C7H5NO4, contains two cations, two anions and two neutral 4-nitrobenzoic acid molecules. In the crystal, O—H...O, N—H...O and C—H...O hydrogen bonds connect the ions and molecules, forming a three-dimensional network.
Muhammad Athar Abbasi +5 more
openaire +1 more source
The perfoliate pondweed, Potamogeton perfoliatus, is a common macrophyte in freshwater and subarctic coastal areas. This species builds extensive meadows that play a role as a filter removing nutrients traversing from land to sea and maintaining essential ecosystem functions.
Kesava Priyan Ramasamy +4 more
wiley +1 more source
Bioavailability of pollutants and chemotaxis [PDF]
The exposure of bacteria to pollutants induces frequently chemoattraction or chemorepellent reactions. Recent research suggests that the capacity to degrade a toxic compound has co-evolved in some bacteria with the capacity to chemotactically react to it.
Jimenez-Sanchez, Celia +5 more
core +2 more sources
A new type of hydrogen-bond pattern for piperidinium p-substituted benzoates is reported; this is found in piperidinium p-nitrobenzoate, C5H12N+·C7H4NO4−, (I). In the crystal of (I), the cations and anions are linked by N—H⋯O hydrogen bonds around a center of symmetry to form a cyclic dimer of the formula unit.
Yoshimitsu Moritani +2 more
openaire +1 more source
Cold‐adapted Rhodococcus sp. strain R1B_2T from Arctic Tupirvik Beach (Northwest Passage) degrades short‐ to long‐chain hydrocarbons in summer seawater (−1°C to 5°C) via a synergistic activity of key hydrocarbon degradation genes (alkB, CYP153, almA, and ladA), with rhlABCR‐linked rhamnolipid production supporting biodegradation.
Nastasia J. Freyria +4 more
wiley +1 more source
Synthesis of Circumpyrene by Alkyne Benzannulation of Brominated Dibenzo[hi,st]ovalene [PDF]
A transition-metal catalyzed alkyne benzannulation allowed an unprecedented synthesis of circumpyrene, starting from 3,11-dibromo-6,14-dimesityldibenzo[hi,st]ovalene (DBOV).
Akimitsu Narita +3 more
core +2 more sources
Benzyl 2,6-dihydroxy-3-nitrobenzoate
Crystals of the title compound, C14H11NO6, were obtained by the reaction of benzyl 2,6-dihydroxybenzoate with nitric acid and crystallization of the product from ethyl acetate. In the molecule, the nitro group is essentially coplanar with the attached benzene ring [O—N—C—C = 176.75 (11)°], indicating conjugation with the π-electron system.
Vijayakumar N. Sonar +3 more
openaire +1 more source

