Synthesis and in Silico Study of Novel Benzisoxazole‐Chromene Derivatives as Potent Inhibitors of Acetylcholinesterase: Metal‐Free Site‐Selective C−N Bond Formation via Aza‐Michael Reaction DOI
Grace Victoria Govada, Sabbasani Rajasekhara Reddy

Chemistry & Biodiversity, Journal Year: 2023, Volume and Issue: 20(8)

Published: July 7, 2023

Abstract An efficient metal‐free approach for site selective C−N coupling reaction of benzo[d]isoxazole and 2 H ‐chromene derivatives has been designed developed against AchE. This nitrogen containing organo‐base promoted methodology, which is both practical environmentally friendly, provides an easy suitable pathway synthesizing Benzisoxazole‐Chromene (BC) possessing poly heteroaryl moieties. The synthesized BC 4 a – n was docked into the active sites AChE to obtain more perception binding modes compounds. Out them, compound l displayed potent activity high selectivity inhibition. Final docking results indicates that showed lowest energy −11.2260 kcal/mol with AChE. analogs would be potential candidates promoting studies in medicinal chemistry research.

Language: Английский

Synthesis of functionalized S-benzyl dithiocarbamates from diazo-compounds via multi-component reactions with carbon disulfide and secondary amines DOI
Nitin Kumar, Rapelly Venkatesh, Jeyakumar Kandasamy

et al.

Organic & Biomolecular Chemistry, Journal Year: 2022, Volume and Issue: 20(34), P. 6766 - 6770

Published: Jan. 1, 2022

Triflic acid promoted multicomponent synthesis of functionalized S -benzyl dithiocarbamates from diazo compounds and secondary amines in the presence carbon disulfide is described.

Language: Английский

Citations

13

S-Alkylation of dithiocarbamates via a hydrogen borrowing reaction strategy using alcohols as alkylating agents DOI

P. Hima,

Spandan Hati, Raju Dey

et al.

Organic & Biomolecular Chemistry, Journal Year: 2023, Volume and Issue: 21(31), P. 6360 - 6367

Published: Jan. 1, 2023

S -Alkylation of dithiocarbamates using alcohols as alkylating agents via a hydrogen borrowing strategy hydroxyapatite-supported copper nanoparticles heterogeneous catalyst.

Language: Английский

Citations

7

Fe SAC on Nitrogen‐Doped Carbon: An Efficient Catalyst for S‐Alkylation of Dithiocarbamates via Borrowing Hydrogen Strategy DOI Creative Commons

M. Vageesh,

P. Hima,

P. A. Bhobe

et al.

Asian Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 13(5)

Published: March 7, 2024

Abstract Herein we report, the synthesis of single‐atom iron on nitrogen‐doped carbon as a catalyst for direct formation C sp3 −S bond via borrowing hydrogen strategy using alcohols alkylating agent. The was synthesized by encapsulating ferrocene within ZIF‐8 framework, followed pyrolysis and characterized precisely FE‐SEM, HR‐TEM, XPS, Raman, XRD EXAFS. is robust, displayed an excellent reactivity in reaction could be recycled five times without any appreciable loss activity.

Language: Английский

Citations

2

Synthesis and Antibacterial Activity Test of Dibutyl Tin (IV) N-Ethylbenzyl Dithiocarbamate Compound Against Salmonella Thy.Atcc.14028 and Propionibacterium acnes Bacteria DOI Creative Commons
Mukhlis Sanuddin,

Medi Andriani,

Tiara Angraini

et al.

Jurnal Kimia Sains dan Aplikasi, Journal Year: 2024, Volume and Issue: 27(7), P. 300 - 306

Published: May 28, 2024

The complex compound dithiocarbamate exhibits various biological activities, including anticancer, antibacterial, antifungal, and antioxidant properties. Dibutyl tin (IV) N-ethyl benzyl was synthesized to overview its structure evaluate antibacterial activity against Salmonella typhimurium ATCC 14028 Propionibacterium acnes. This via an in situ method by adding dibutyl dichloride, N-ethylbenzylamine, carbon disulfide, forming a precipitate, which then dried yield white powder. powder can also be crystallized. characterized using FTIR, 1H NMR, 13C NMR spectroscopy, along with testing the disc diffusion method. FTIR analysis revealed characteristic absorption bands at 1111.00 cm-1 (C-N), 731.02 (C-S), 2954.95 (C-H), 1602.85 (C=C), 360.69 (Sn-S), 567.07 (Sn-C). spectrum showed chemical shifts 0-3.8570 ppm (δ CH3), 5.0032-5.1472 N-CH2), 7.2780-7.3607 C6H5). displayed signals 0-34.5610 48.6398-56.9247 127.6651-135.7665 C6H5), 201.7568 CS2). of assessed, revealing inhibition zones typhi 6.78 mm (100 ppm), 7.36 (120 7.76 (140 categorizing as moderate. Against acnes, were 1.8 1.88 2.13 weak. Based on these findings, it concluded that form octahedral activity. However, is not yet suitable for use new antibiotic.

Language: Английский

Citations

1

Ultrasound-assisted ring opening of epoxides in HFIP: THF: Synthesis, characterization, computational studies and molecular docking of novel 2‑hydroxy dithiocarbamates DOI
Vishal Sharma,

Manisha Nidhar,

Muhammad Sheraj

et al.

Journal of Molecular Structure, Journal Year: 2024, Volume and Issue: 1318, P. 139212 - 139212

Published: July 6, 2024

Language: Английский

Citations

1

TfOH-catalyzed three-component synthesis of Dithiocarbamates from α-Diazoesters under continuous flow conditions DOI
Rui Wang,

Hangli He,

Qiongjiao Yan

et al.

Journal of Flow Chemistry, Journal Year: 2022, Volume and Issue: 13(1), P. 1 - 8

Published: Dec. 12, 2022

Language: Английский

Citations

6

Formation of lignin alkyl-O-alkyl ether structures via 1,6-addition of aliphatic alcohols to β-O-4-aryl ether quinone methides DOI
Xuhai Zhu, Dazhi Zhang, Rui Lu

et al.

Organic & Biomolecular Chemistry, Journal Year: 2023, Volume and Issue: 21(28), P. 5840 - 5854

Published: Jan. 1, 2023

In this work, diastereo-preferential formation of alkyl-O-alkyl ether structures via 1,6-addition alcohols to β-O-4-aryl quinone methides was studied.

Language: Английский

Citations

3

Synthesis of new dithiocarbamate and xanthate complexes and their application in enrichment processes DOI Creative Commons
А. Е. Бурдонов,

Надежда В. Вчисло,

Екатерина А. Верочкина

et al.

Proceedings of universities Applied chemistry and biotechnology, Journal Year: 2023, Volume and Issue: 13(2), P. 160 - 171

Published: July 1, 2023

Ore flotation is the main and defining technological process in ore benefication non-ferrous metals production. The requires use of a variety chemical reagents, including collectors, frothers, surface modifiers, pH regulators. development selection suitable reagents for processed material play vital role efficient flotation. activity collectors depends fundamentally on composition structure hydrophobic hydrophilic fragments forming agent molecule, as well nature that undergoes processing. In this regard, identification study “substance structure–flotation activity” relation, search new effective gain importance within applied organic organoelement chemistry related branches science technology. article, we review syntheses collector namely xanthates dithiocarbamates, based literature data past five years. Where necessary, earlier sources are provided. reaction conditions yields target compounds presented using schemes. addition, present results tests surfaces various ores mechanism concentrate extraction. According to reviewed publications, fixation minerals can be regarded complexation functional groups metal ions located mineral.

Language: Английский

Citations

2

Base-mediated synthesis of cyclic dithiocarbamates from 1-amino-3-chloropropan-2-ol derivatives and carbon disulfide DOI
Yasunori Toda,

Masaya Iwasaki,

Hiroyuki Suga

et al.

Organic & Biomolecular Chemistry, Journal Year: 2023, Volume and Issue: 21(31), P. 6293 - 6297

Published: Jan. 1, 2023

An efficient method for the preparation of six-membered cyclic dithiocarbamates is described, in which triethylamine effectively promotes reaction 1-amino-3-chloropropan-2-ol derivatives with carbon disulfide. On basis experimental and theoretical studies, a mechanism proposed to explain difference between present our previously reported dioxide fixation.

Language: Английский

Citations

2

Acid‐Catalyzed Regioselective Synthesis of α‐Diarylmethyl Substituted Phenols and para‐Quinone Methides in Water DOI
Biquan Xiong,

Wenli Shang,

Weifeng Xu

et al.

Asian Journal of Organic Chemistry, Journal Year: 2022, Volume and Issue: 11(8)

Published: July 2, 2022

Abstract A facile and efficient method for the synthesis of α ‐diarylmethyl substituted phenols from para ‐quinone methides ( p ‐QMs) with has been developed by using phosphoric acid as catalyst water green solvent under mild conditions. In addition, when TEMPO was added an additive reaction, diaryl‐substituted could be generated target product. The reactions show high functional group tolerance, good to excellent yields unique selectivity, a broad range motif containing phenol(s) quinones prepared through divergent methods. Furthermore, series control experiments were performed gain insights plausible mechanisms. These protocols have atomic economy, may significant implications construction C( sp 3 )−C( 2 ) bonds in organic synthesis.

Language: Английский

Citations

4