One-Pot Sequential Synthesis of Alkenylated Dihydroquinolinones and Hexahydroacridinones in Deep Eutectic Solvent Medium DOI Creative Commons

Sundararajan Suresh,

Fazlur‐Rahman Nawaz Khan

ACS Omega, Journal Year: 2024, Volume and Issue: unknown

Published: Aug. 16, 2024

The sequential synthesis of N-heterocycles from saturated ketones poses significant challenges and has rarely been reported. Herein, an efficient alkenylated dihydroquinolinones 7 hexahydroacridinones 8 is achieved 1 or 2 via dehydrogenation, cyclization, oxidation, α-alkenylation in choline chloride-based deep eutectic solvent (DES) medium. This strategy provides excellent yield low-cost, readily available starting materials under environmentally benign conditions. Furthermore, the synthesized compounds (4, 5, 7, 8) were investigated for their photophysical properties through absorption emission spectral studies.

Language: Английский

Photoredox/NHC cooperative catalysis for alkylacylation of styrenes: An alternative method for the synthesis of γ-aminoketones DOI

Ke-Yang Yu,

Fu Cheng,

Dong-Sen Duan

et al.

Tetrahedron Letters, Journal Year: 2025, Volume and Issue: 156, P. 155450 - 155450

Published: Jan. 8, 2025

Language: Английский

Citations

1

Cu(ii)-catalyzed synthesis of N-sulfonated quinolin-2(1H)-one-3-carboxamides DOI
Xue Chen, Sheng Fang, Quan Zhou

et al.

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

Herein, we present an efficient Cu( ii )-catalyzed cascade synthesis of sulfonated 3-carboxamide quinolin-2-(1 H )-ones. Inthis paper, sulfonylhydrazides underwent unusual N–N bond cleavage and functioned as sulfamide synthons.

Language: Английский

Citations

3

Carbonylative Cyclization of Biaryl Enones with Aldehydes and Oxamic Acids DOI
Chada Raji Reddy, Dattahari H. Kolgave,

Sana Fatima

et al.

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(24), P. 4901 - 4911

Published: Jan. 1, 2024

An oxidative radical-promoted carbonylative cyclization strategy for the synthesis of phenanthren-9-(10

Language: Английский

Citations

1

Metal-Free Synthesis of Pharmaceutically Relevant Sulfonylureas via Direct Reaction of Sulfonamides with Amides DOI

Sahil Mondal,

Rakhi Sati,

Muhammed F. Hashim

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(18), P. 13179 - 13191

Published: Aug. 28, 2024

A metal-free process has been developed for the sustainable synthesis of medicinally important sulfonylureas in one pot via direct reaction sulfonamides with amides green solvent (DMC). The proceeded efficiently at room temperature, and products were obtained good to excellent yields. use readily accessible, inexpensive, environmentally benign starting materials reagents, mild conditions, wide substrate scope, tolerance air moisture, operational simplicity, atom economy are salient features this protocol. Gram-scale antidiabetic drugs tolbutamide chlorpropamide yields further revealed practical utility procedure. Additionally, synthetic value straightforward method is showcased by late-stage modification drug molecules, including drug-drug conjugation Preliminary mechanistic studies indicated

Language: Английский

Citations

1

Synthesis of succinyldiamides containing all-quaternary carbon center by photo-induced amidation/smiles rearrangement of alkenes DOI
Yuyu Dai, Wei Niu, Jiapeng Huang

et al.

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 23, 2024

A novel, mild, and environmentally friendly method was developed for the synthesis of quaternary-carbon-containing succinyldiamides. This found to be compatible with many substrates.

Language: Английский

Citations

1

One-Pot Sequential Synthesis of Alkenylated Dihydroquinolinones and Hexahydroacridinones in Deep Eutectic Solvent Medium DOI Creative Commons

Sundararajan Suresh,

Fazlur‐Rahman Nawaz Khan

ACS Omega, Journal Year: 2024, Volume and Issue: unknown

Published: Aug. 16, 2024

The sequential synthesis of N-heterocycles from saturated ketones poses significant challenges and has rarely been reported. Herein, an efficient alkenylated dihydroquinolinones 7 hexahydroacridinones 8 is achieved 1 or 2 via dehydrogenation, cyclization, oxidation, α-alkenylation in choline chloride-based deep eutectic solvent (DES) medium. This strategy provides excellent yield low-cost, readily available starting materials under environmentally benign conditions. Furthermore, the synthesized compounds (4, 5, 7, 8) were investigated for their photophysical properties through absorption emission spectral studies.

Language: Английский

Citations

0