{"title":"面向多样性,一步合成铬二甲基[2,3-]","authors":"]Indoles and Thiochromeno[2,3-","doi":"10.3987/com-23-14920","DOIUrl":null,"url":null,"abstract":"<span>A general and efficient synthesis of tetracyclic chromeno[2,3-</span><span>b</span><span>]indoles, thiochromeno[2,3-</span><span>b</span><span>]indoles and 6</span><span>H</span><span>-indolo[2,3-</span><span>b</span><span>]quinolines has been achieved through a microwave-assisted, metal free, base catalyzed domino Knoevenagel condensation, intramolecular cyclization process starting from simple indoline-2-thiones and 2-substituted benzaldehyde derivatives. This approach provides a straightforward, atom economical and concise route to access a range of otherwise not easily available heterocycles in good yields.<br/></span>","PeriodicalId":13166,"journal":{"name":"Heterocycles","volume":"136 5","pages":""},"PeriodicalIF":0.8000,"publicationDate":"2023-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Diversity-Oriented, One Step Synthesis of Chromeno[2,3-\",\"authors\":\"]Indoles and Thiochromeno[2,3-\",\"doi\":\"10.3987/com-23-14920\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<span>A general and efficient synthesis of tetracyclic chromeno[2,3-</span><span>b</span><span>]indoles, thiochromeno[2,3-</span><span>b</span><span>]indoles and 6</span><span>H</span><span>-indolo[2,3-</span><span>b</span><span>]quinolines has been achieved through a microwave-assisted, metal free, base catalyzed domino Knoevenagel condensation, intramolecular cyclization process starting from simple indoline-2-thiones and 2-substituted benzaldehyde derivatives. This approach provides a straightforward, atom economical and concise route to access a range of otherwise not easily available heterocycles in good yields.<br/></span>\",\"PeriodicalId\":13166,\"journal\":{\"name\":\"Heterocycles\",\"volume\":\"136 5\",\"pages\":\"\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2023-11-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Heterocycles\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.3987/com-23-14920\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Heterocycles","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.3987/com-23-14920","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Diversity-Oriented, One Step Synthesis of Chromeno[2,3-
A general and efficient synthesis of tetracyclic chromeno[2,3-b]indoles, thiochromeno[2,3-b]indoles and 6H-indolo[2,3-b]quinolines has been achieved through a microwave-assisted, metal free, base catalyzed domino Knoevenagel condensation, intramolecular cyclization process starting from simple indoline-2-thiones and 2-substituted benzaldehyde derivatives. This approach provides a straightforward, atom economical and concise route to access a range of otherwise not easily available heterocycles in good yields.
期刊介绍:
Since its inception in 1973 HETEROCYCLES has provided a platform for the rapid exchange of research in the areas of organic, pharmaceutical, analytical, and medicinal chemistry of heterocyclic compounds in addition to communications, papers, reviews, a special section of the journal presents newly-discovered natural products whose structure has recently been established.
Another section is devoted to the total synthesis of previously documented natural products with heterocyclic ring systems.
Due to the fact that the journal is able to publish articles within two months of receipt of the manuscripts, researchers in this field can obtain up-to-date information on heterocyclic research by reading Heterocycles regularly.
Audience: Organic and Physical Organic Chemists, Biochemists, Pharmacologists and Scientists studying heterocyclic compounds