Organocatalytic Enantioselective Chloroiminocyclization for the Synthesis of Imidazoline DOI
Qifeng Guo,

Zhitao Lai,

Tian Zeng

et al.

Organic Letters, Journal Year: 2024, Volume and Issue: 26(26), P. 5592 - 5596

Published: June 24, 2024

Imidazoline is an important scaffold in organic synthesis and a pharmacophore medicinal chemistry. We apply basic imines as nucleophiles for the catalytic asymmetric chloroiminocyclization to furnish tetrasubstituted stereocenter-containing imidazolines excellent yields enantioselectivities. The reaction can be conducted polar solvent acetonitrile under concentrated conditions.

Language: Английский

Chitosan-based Schiff bases: Promising materials for biomedical and industrial applications DOI

Varun Pawariya,

Soumik De, Joydeep Dutta

et al.

Carbohydrate Polymers, Journal Year: 2023, Volume and Issue: 323, P. 121395 - 121395

Published: Sept. 16, 2023

Language: Английский

Citations

57

Mechanistic insight into the synergistic role of the dual-surfactant system as a green solvent for deoximation reaction: An experimental and computational analysis DOI
Soumik De, Mona Sunaydih Alsaeedi, Debadutta Das

et al.

Journal of Molecular Liquids, Journal Year: 2024, Volume and Issue: 400, P. 124559 - 124559

Published: March 26, 2024

Language: Английский

Citations

10

Synthesis and characterization of a new developed modified-chitosan Schiff base with improved antibacterial properties for the removal of Bismarck Brown R and Eosin Y dyes from wastewater DOI Creative Commons

Varun Pawariya,

Soumik De, Joydeep Dutta

et al.

Carbohydrate Polymer Technologies and Applications, Journal Year: 2023, Volume and Issue: 6, P. 100352 - 100352

Published: Aug. 18, 2023

In this study, the synthesis of a new chitosan-based Schiff base with surface modification using chloroethanoic acid was reported. The physicochemical attributes modified chitosan were studied. characterized X-ray diffraction (XRD) technique; Fourier transform infrared (FTIR) and UV-visible spectroscopies; thermogravimetric analysis; differential scanning calorimetry (DSC). Bruner-Emmett-Teller (BET) analysis performed to determine area synthesized compound electron microscope (SEM) characterize its morphology. adsorption efficacy Bismarck Brown R evaluated through multilayer formation, whereas Eosin Y adsorbed onto homogenous formation monolayer. Additionally, base's for BBR EY dye calculated be 327 mg/g 386 mg/g, respectively. effectively inhibited both gram positive negative bacteria, thus, exhibiting antibacterial properties. results showed that could used remove dyes from wastewater.

Language: Английский

Citations

20

Total Synthesis of Natural Products using Gold Catalysis DOI
Soumik De, Aritra Kumar Dan, Raghaba Sahu

et al.

Chemistry - An Asian Journal, Journal Year: 2022, Volume and Issue: 17(24)

Published: Oct. 18, 2022

Gold catalysis is an extremely enthusiastic field of investigation in the area. The development alternative, highly inventive, precompetitive techniques based on gold has paved way for executing a broad spectrum chemical transformations from uncomplicated starting materials. total synthesis natural products complex and more complicated task. An amalgamation product through gold-catalysis been thought-provoking job. protocol solved several problems related to numerous products. Thus, this review outlined some most notable benchmarks last seven years (2015-2021) their application strategy acquired by authors accomplish will be elaborately discussed emphasizing role gold-catalyzed reactions.

Language: Английский

Citations

22

Self-Assembled Micellar Saponin from Sapindus laurifolia Vahl.: Investigations on the Surfactant Activity on the Extraction of Fibroin from Silk Cocoons DOI

Bhagyashree Biswal,

Aritra Kumar Dan, Bari Aamna

et al.

Journal of Polymers and the Environment, Journal Year: 2023, Volume and Issue: 31(9), P. 3803 - 3813

Published: April 15, 2023

Language: Английский

Citations

13

Salicylaldehyde-diphenyl-azine skeleton-based ESIPT-coupled AIEgens with tunable emission and applicable as highly selective and sensitive Cu2+ ion sensor DOI
Abhinav Jain, Soumik De, Pranjit Barman

et al.

Dyes and Pigments, Journal Year: 2023, Volume and Issue: 220, P. 111769 - 111769

Published: Oct. 21, 2023

Language: Английский

Citations

12

The literature of heterocyclic chemistry, part XXII, 2022 DOI
Галина А. Газиева, Yu. B. Evdokimenkova, N. O. Soboleva

et al.

Advances in heterocyclic chemistry, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Language: Английский

Citations

0

Asymmetric Synthesis of α-Spiro-γ-lactones and α-Substituted γ-Lactones via Chiral Bifunctional Sulfide-Catalyzed Bromolactonizations DOI

Taiki Mori,

Koki Abe,

Seiji Shirakawa

et al.

The Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 88(12), P. 7830 - 7838

Published: Jan. 25, 2023

An efficient enantioselective synthesis of γ-chiral α-spiro-γ-lactones, which are important building blocks for pharmaceuticals, was achieved via BINOL-derived chiral bifunctional sulfide-catalyzed bromolactonizations α-allyl carboxylic acids containing either hetero- or carbocyclic structures. Transformations the resultant α-spiro-type bromolactonization product were examined to obtain optically active γ-functionalized α-spiro-γ-lactones. The utility this catalytic system also demonstrated in asymmetric α,α-diaryl- and dialkyl-substituted γ-lactones.

Language: Английский

Citations

9

Synthesis, SAR, and application of JQ1 analogs as PROTACs for cancer therapy DOI
Soumik De, Raghaba Sahu, Shubhendu Palei

et al.

Bioorganic & Medicinal Chemistry, Journal Year: 2024, Volume and Issue: 112, P. 117875 - 117875

Published: Aug. 16, 2024

Language: Английский

Citations

2

Enantioselective Synthesis of Bromodifluoromethyl‐containing Oxazolines by Concerted Lewis/Brønsted Base Catalysis with Chiral Bisphosphine Oxide DOI

Ryo Hirokawa,

Yuki NAKAHARA,

Shotaro Uchida

et al.

Chemistry - An Asian Journal, Journal Year: 2023, Volume and Issue: 18(8)

Published: Feb. 25, 2023

We describe regio- and enantioselective bromocyclization of difluoroalkenes catalyzed by chiral bisphosphine oxides. Owing to the simultaneous activation both brominating reagent amide substrate, desired cyclization reaction proceeds smoothly even at low temperature provide bromodifluoromethyl-containing oxazolines with a quaternary center in highly fashion (up 99% ee). This protocol features use commercially available reagents readily accessible catalysts. The regioselectivity enantioselectivity are influenced catalyst structure, reagent, temperature. Under optimal conditions, 5-exo preferentially compared 6-endo cyclization, depending on electronic properties alkene substrates. A gram-scale synthesis oxazoline was achieved as little 1 mol % catalyst.

Language: Английский

Citations

4