Synthesis and biological evaluation of novel benzo[a]pyridazino[3,4-c]phenazine derivatives DOI
Le Nhat Thuy Giang, Tuyet Anh Dang Thi, Quynh Giang Nguyen Thi

и другие.

Bioorganic & Medicinal Chemistry Letters, Год журнала: 2021, Номер 43, С. 128054 - 128054

Опубликована: Апрель 22, 2021

Язык: Английский

Microwave-Assisted Green Synthesis, In Silico Study, and Plant Growth Stimulant Activity of Novel 3-(2-Arylidenehydrazinyl)-6-chloropyridazines DOI
Emma A. Ghazaryan, T. A. Gomktsyan, A. V. Karapetyan

и другие.

Russian Journal of General Chemistry, Год журнала: 2025, Номер 95(3), С. 704 - 714

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

A concise and focused overview upon arylglyoxal monohydrates-based one-pot multi-component synthesis of fascinating potentially biologically active pyridazines DOI
Hossein Mousavi

Journal of Molecular Structure, Год журнала: 2021, Номер 1251, С. 131742 - 131742

Опубликована: Окт. 19, 2021

Язык: Английский

Процитировано

24

N,N,N’,N’-Tetramethylethylenediamine-Enabled Photoredox-Catalyzed C–H Methylation of N-Heteroarenes DOI
Fang Liu,

Zhipeng Ye,

Yuan‐Zhuo Hu

и другие.

The Journal of Organic Chemistry, Год журнала: 2021, Номер 86(17), С. 11905 - 11914

Опубликована: Авг. 3, 2021

Aiming at the valuable methylation process, readily available and inexpensive N,N,N',N'-tetramethylethylenediamine (TMEDA) was first identified as a new methyl source in photoredox-catalyzed transformation this work. By virtue of simple methylating reagent, facile practical protocol for direct C-H N-heteroarenes developed, featuring mild reaction conditions, broad substrate scope, scalability. Mechanistic studies disclosed that sequential photoredox, base-assisted proton shift, fragmentation, tautomerization process essentially involved.

Язык: Английский

Процитировано

23

Bacterial Hydrazine Biosynthetic Pathways Featuring Cupin/Methionyl tRNA Synthetase‐like Enzymes DOI
Kenichi Matsuda, Toshiyuki Wakimoto

ChemBioChem, Год журнала: 2024, Номер 25(9)

Опубликована: Март 9, 2024

Nitrogen-Nitrogen (N-N) bond-containing functional groups in natural products and synthetic drugs play significant roles exerting biological activities. The mechanisms of N-N bond formation organic molecules have garnered increasing attention over the decades. Recent advances illuminated various enzymatic nonenzymatic strategies, our understanding construction is rapidly expanding. A group didomain proteins with zinc-binding cupin/methionyl-tRNA synthetase (MetRS)-like domains, also known as hydrazine synthetases, generates amino acid-based hydrazines, which serve key biosynthetic precursors diverse functionalities such hydrazone, diazo, triazene, pyrazole, pyridazinone groups. In this review, we summarize current knowledge on pathways employing unique bond-forming machinery.

Язык: Английский

Процитировано

3

Synthesis and biological evaluation of novel benzo[a]pyridazino[3,4-c]phenazine derivatives DOI
Le Nhat Thuy Giang, Tuyet Anh Dang Thi, Quynh Giang Nguyen Thi

и другие.

Bioorganic & Medicinal Chemistry Letters, Год журнала: 2021, Номер 43, С. 128054 - 128054

Опубликована: Апрель 22, 2021

Язык: Английский

Процитировано

19