Reactions of 2-aminothiphenols with chalcones in an ionic liquid medium: a chemoselective catalyst-free synthesis of 1,5-benzothiazepines-Reference-Cited by-同舟云学术

Reactions of 2-aminothiphenols with chalcones in an ionic liquid medium: a chemoselective catalyst-free synthesis of 1,5-benzothiazepines

Published:2015-03-04 Issue:3 Volume:36 Page:257-269
ISSN:1741-5993
Container-title:Journal of Sulfur Chemistry
language:en
Short-container-title:Journal of Sulfur Chemistry

Author:

Sharifi Ali¹,Hosseini Fahimeh¹,Ghonouei Nima¹,Abaee M. Saeed¹,Mirzaei Mojtaba¹,Mesbah A. Wahid¹,Harms Klaus²

Affiliation:

1. Department of Organic Chemistry and Natural Products, Chemistry and Chemical Engineering Research Center of Iran, Pajouhesh Blvd, 17th Km Tehran-Karaj Highway, P.O. Box 14335-186, Tehran, Iran

2. Fachbereich Chemie der Philipps-Universitaet Marburg, Hans-Meerwein-Strasse, Marburg D-35032, Germany

Publisher

Informa UK Limited

Subject

General Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/17415993.2015.1014483

Reference43 articles.

1. Ionic Liquids in Synthesis

2. Room-Temperature Ionic Liquids: Solvents for Synthesis and Catalysis. 2

3. Ionic Liquids

4. Structure and Solvation in Ionic Liquids

5. Ionic Liquids in Heterocyclic Synthesis

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Investigation on the pharmacological profile for new synthesized bis heterocyclic analogs containing nitrogen atom as anti-cancer therapy target;Journal of Molecular Structure;2024-09

2. Synthesis and Biological Evaluation of Benzothiazepine, Benzothiazole, and Benzothiophene Derivatives;S-Heterocycles;2024

3. A versatile switching method for N- or O-alkylation of 2-aminophenols using ionic liquids: Selective access to benzo[1,4]oxazine-2-one and benzo[1,4]oxazine-3-one derivatives;Tetrahedron Letters;2023-08

4. 1,5-Benzothiazepines: Recent developments in the synthetic strategies;Tetrahedron;2023-08

5. Synthesis of the 1,5‐Benzothiazepane Scaffold – Established Methods and New Developments;ChemistryOpen;2023-02