Leila Kavoosi, Bagher Aghamiri, F. Matloubi Moghaddam
{"title":"区域选择性和非对映选择性合成吲哚喹啉-噻唑烷-2-硫酮和双吲哚喹啉-二氨基二硫酸衍生物,并研究其光致发光性质和潜在应用","authors":"Leila Kavoosi, Bagher Aghamiri, F. Matloubi Moghaddam","doi":"10.1016/j.tet.2025.134708","DOIUrl":null,"url":null,"abstract":"<div><div>This study presents a regio- and diastereoselective method for synthesizing indeno-quinoxaline-thiazolidine-2-thione and bis-indeno-quinoxaline-dicarbamodithioate hybrids. The target compounds are synthesized via a one-pot reaction of carbon disulfide, various amines, and 2-(11<em>H</em>-indeno [1,2-<em>b</em>]quinoxalin-11-ylidene)-1-phenylethan-1-one derivatives. The reaction proceeds under mild conditions, affording the products in high yields with high selectivity. The protocol is operationally simple and has been demonstrated on a gram scale, indicating its suitability for large-scale synthesis and compound library generation. Additionally, the synthesized hybrids exhibit photoluminescent properties, which may be of interest for further interdisciplinary investigation.</div></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":"183 ","pages":"Article 134708"},"PeriodicalIF":2.1000,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Regio- and diastereoselective synthesis of indeno-quinoxaline-thiazolidine-2-thione and bis-indeno-quinoxaline-dicarbamodithioate derivatives, along with an investigation of their photoluminescent properties and potential applications\",\"authors\":\"Leila Kavoosi, Bagher Aghamiri, F. Matloubi Moghaddam\",\"doi\":\"10.1016/j.tet.2025.134708\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study presents a regio- and diastereoselective method for synthesizing indeno-quinoxaline-thiazolidine-2-thione and bis-indeno-quinoxaline-dicarbamodithioate hybrids. The target compounds are synthesized via a one-pot reaction of carbon disulfide, various amines, and 2-(11<em>H</em>-indeno [1,2-<em>b</em>]quinoxalin-11-ylidene)-1-phenylethan-1-one derivatives. The reaction proceeds under mild conditions, affording the products in high yields with high selectivity. The protocol is operationally simple and has been demonstrated on a gram scale, indicating its suitability for large-scale synthesis and compound library generation. Additionally, the synthesized hybrids exhibit photoluminescent properties, which may be of interest for further interdisciplinary investigation.</div></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":\"183 \",\"pages\":\"Article 134708\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-05-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0040402025002649\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040402025002649","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Regio- and diastereoselective synthesis of indeno-quinoxaline-thiazolidine-2-thione and bis-indeno-quinoxaline-dicarbamodithioate derivatives, along with an investigation of their photoluminescent properties and potential applications
This study presents a regio- and diastereoselective method for synthesizing indeno-quinoxaline-thiazolidine-2-thione and bis-indeno-quinoxaline-dicarbamodithioate hybrids. The target compounds are synthesized via a one-pot reaction of carbon disulfide, various amines, and 2-(11H-indeno [1,2-b]quinoxalin-11-ylidene)-1-phenylethan-1-one derivatives. The reaction proceeds under mild conditions, affording the products in high yields with high selectivity. The protocol is operationally simple and has been demonstrated on a gram scale, indicating its suitability for large-scale synthesis and compound library generation. Additionally, the synthesized hybrids exhibit photoluminescent properties, which may be of interest for further interdisciplinary investigation.
期刊介绍:
Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry.
Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters.
Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.