Journal of Fluorine Chemistry, Год журнала: 2024, Номер unknown, С. 110372 - 110372
Опубликована: Ноя. 1, 2024
Язык: Английский
Journal of Fluorine Chemistry, Год журнала: 2024, Номер unknown, С. 110372 - 110372
Опубликована: Ноя. 1, 2024
Язык: Английский
International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(3), С. 1103 - 1103
Опубликована: Янв. 27, 2025
Plant viral diseases cause great harm to crops in terms of yield and quality. Natural products have been providing an excellent source novel chemistry, inspiring the development synthetic pesticides. The Amaryllidaceae alkaloids crinasiadine (3a), trisphaeridine (4a), bicolorine (5a) were selected as parent structures, a series their derivatives designed, synthesized, investigated for anti-plant virus effects first time. Compounds 13b 18 exhibited comparable inhibitory activities ningnanmycin against tobacco mosaic (TMV). Preliminary research into mechanism, involving transmission electron microscopy molecular docking studies, suggests that compound may interfere with elongation phase TMV assembly process. This study provides some important information agrochemicals phenanthridine structures.
Язык: Английский
Процитировано
1The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Янв. 13, 2025
A photoredox-promoted cascade glycosylation/cyclization reaction of 2-isocyanobiaryls and glycosyl NHP esters was established for the synthesis nonclassical heteroaryl C-glycosides. This methodology is characterized by an exceedingly simple system, high diastereoselectivity, good functional group tolerance. In contrast to traditional strategies, this innovative approach circumvents need temperature, transition metal, photocatalyst, offering environmentally friendly efficient protocol.
Язык: Английский
Процитировано
0Organic Chemistry Frontiers, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
We reported the first example of visible-light-induced radical cascade cyclization 2-isocyanobiaryls via 1,5-HAT, which is characterized by broad substrate scope, excellent functional group compatibility and no requirement any metals base.
Язык: Английский
Процитировано
0Chinese Journal of Chemistry, Год журнала: 2024, Номер unknown
Опубликована: Сен. 10, 2024
Comprehensive Summary A visible‐light‐induced decarboxylative radical cascade cyclization reaction between N ‐(2‐cyanoaryl)‐acrylamides and alkyl ‐(acyloxy)phthalimide (NHPI esters) for the construction of phenanthridine derivatives has been developed. This approach utilizes lithium iodide (LiI) triphenylphosphine (PPh 3 ) as redox catalysts is produced through photoactivation electron donor‐acceptor (EDA) complex. series primary, secondary, tertiary alkyl‐substituted phenanthridines are prepared in up to 82% yield without transition‐metal catalysts, chemical oxidants, or metal‐/organic dye‐based photocatalysts.
Язык: Английский
Процитировано
1Organic Chemistry Frontiers, Год журнала: 2024, Номер unknown
Опубликована: Ноя. 13, 2024
Development of novel and efficient synthetic methods to achieve valuable N-heterocycles from aryldiazonium salts has been an important research area in organic chemistry for several decades.
Язык: Английский
Процитировано
1Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(29), С. 5982 - 5986
Опубликована: Янв. 1, 2024
An unprecedented trifunctionalization of CC bonds in 2-(1-azidovinyl)-1,1'-biphenyls has been successfully achieved using the NCS/AgNO
Язык: Английский
Процитировано
0The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(20), С. 15117 - 15136
Опубликована: Окт. 1, 2024
This study introduces a straightforward synthetic approach for generating 7,8-dihydrobenzo[
Язык: Английский
Процитировано
0Journal of Fluorine Chemistry, Год журнала: 2024, Номер unknown, С. 110372 - 110372
Опубликована: Ноя. 1, 2024
Язык: Английский
Процитировано
0