Results 41 to 50 of about 2,622 (202)

Stereoretentive Nucleophilic Aromatic Substitution Accesses Atropisomeric 4‐Amino‐N‐Arylquinolinium Salts

open access: yesChemistry – A European Journal, Volume 32, Issue 37, 1 October 2026.
Quinolin‐4‐ones were converted to chloroquinolinium salts, allowing formation of axially chiral aminoquinolinium salts via an enantioretentive SNAr reaction with a variety of amine nucleophiles. The salts have a high rotational barrier, with a racemization half‐life of ∼1000s of years.
Darren Holmes   +5 more
wiley   +1 more source

Acridone alkaloids from the rhizomes of Luvunga scandens (Roxb.) Buch. Ham.

open access: yes, 2018
The ethyl acetate extract of the rhizomes of Luvunga scandens (Roxb.) Buch. - Ham. ex Wight & Arn (Rutaceae) delivered one new acridone alkaloid named Luvungaside A (1) together with three known acridone alkaloids, namely 1,3-dihydroxy-2-methoxy-10 ...
Dinh Tri Mai (689087)   +7 more
core   +1 more source

Chemical Metabolomics: Chemical Biology Tools for Advanced Metabolism Investigations

open access: yesAngewandte Chemie, Volume 138, Issue 23, 1 June 2026.
The human metabolism has been investigated for several millennia. The metabolome is known for a high complexity due to a large number of different metabolites that are present at different concentrations. Metabolomics has been developed as a field to investigate the entire human metabolome and to elucidate disease development mechanisms.
Alejandro Torregrosa‐Chinillach   +4 more
wiley   +2 more sources

From Sourcing to End‐of‐Life: Sustainability Challenges and Opportunities in Organic Bioelectronics

open access: yesAdvanced Science, Volume 13, Issue 51, 14 September 2026.
Organic bioelectronics bridges biology and electronics using organic mixed ionic/electronic conductors. This Perspective addresses sustainability across the full lifecycle of organic bioelectronic materials and devices, offering a framework to guide material sourcing, synthesis, fabrication, application, and end‐of‐life strategies toward bioelectronic ...
Gwennaël Dufil   +3 more
wiley   +1 more source

Anthranilate N-methyltransferase, a branch-point enzyme of acridone biosynthesis

open access: yes, 2008
Acridone alkaloids formed by acridone synthase in Ruta graveolens L. are composed of N-methylanthraniloyl CoA and malonyl CoAs. A 1095 bp cDNA from elicited Ruta cells was expressed in Escherichia coli, and shown to encode S-adenosyl-l-methionine ...
Alfred Baumert   +11 more
core   +1 more source

1-Hydroxy-3,4-dimethoxy-10-methylacridin-9-one

open access: yesIUCrData, 2020
There are two independent molecules in the asymmetric unit of the title compound, C16H15NO4, which was isolated from fruits of Zanthoxylum leprieurii. The atoms of the three rings of each molecule are close to coplanar with the largest deviations from ...
Rodrigo S. A. de Araújo   +5 more
doaj   +1 more source

Acridone studies. XIII. The nature of hexabromoacridone

open access: yes, 1975
Acheson's ?hexabromoacridone?1 is shown to be 1,2,3,4,5,7-hexabromo-9- acridone by a combination of N.M.R. spectroscopy and synthesis from specifically tritiated 9-acridones. In boiling piperidine, the bromines at C 1 and C 3 are replaced.
RH Prager
core   +1 more source

Synthesis and nuclease activity of some 'porphyrin-acridone' hybrid molecules

open access: yes, 1993
A short synthesis of several 'porphyrin-acridone' hybrids 4a-e based on 5-(4-hydroxyphenyl)10,15,20-tris(p-tolyl)porphyrin 1 and observations on their photoinitiated nuclease activity are ...
Maiya, Bhaskar G.   +4 more
core   +1 more source

Phytochemical and Biological Short Review Of Subfamily Aurantioideae. [PDF]

open access: yesRecords of Pharmaceutical & Biomedical Sciences
The subfamily Aurantioideae, belonging to the family Botany Rutaceae, represents one of the most economically and medicinally significant groups of flowering plants distributed throughout tropical and subtropical regions. This subfamily comprises several
Mareena Thabet
doaj   +1 more source

Novel acridone derivatives probed using DFT, including design, synthesis, characterization with anti-oxidant and anti-mitotic screening

open access: yesResults in Chemistry, 2023
Applying the Ullmann synthesis, substituted aniline and o-halobenzoic acids are combined with potassium carbonate and copper powder to produce N- (substituted phenyl) anthranilic acids.
S. Sulthanudeen   +3 more
doaj   +1 more source

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