L. Sobenina, A. Demenev, A. Mikhaleva, A. Ushakov, A. Afonin, O. Petrova, V. Elokhina, K. Volkova, D. Toryashinova, B. Trofimov
{"title":"从吡咯-2-碳硫酸盐中功能化取代1,3-二乙烯基[1,2- c][1,3]吡咯洛噻唑","authors":"L. Sobenina, A. Demenev, A. Mikhaleva, A. Ushakov, A. Afonin, O. Petrova, V. Elokhina, K. Volkova, D. Toryashinova, B. Trofimov","doi":"10.1080/02786110212862","DOIUrl":null,"url":null,"abstract":"The reaction of pyrrole-2-carbodithioates with methylenoactive nitriles and 2-benzoyl-1-bromoacetylene in the KOH-DMSO system leads to functionally substituted pyrrolothiazoles in 59-85% yield.","PeriodicalId":22122,"journal":{"name":"Sulfur Letters","volume":"27 1","pages":"87 - 93"},"PeriodicalIF":0.0000,"publicationDate":"2002-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":"{\"title\":\"Functionally substituted 1,3-diethenyl [1,2- c ][1,3]pyrrolothiazoles from pyrrole-2-carbodithioates\",\"authors\":\"L. Sobenina, A. Demenev, A. Mikhaleva, A. Ushakov, A. Afonin, O. Petrova, V. Elokhina, K. Volkova, D. Toryashinova, B. Trofimov\",\"doi\":\"10.1080/02786110212862\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The reaction of pyrrole-2-carbodithioates with methylenoactive nitriles and 2-benzoyl-1-bromoacetylene in the KOH-DMSO system leads to functionally substituted pyrrolothiazoles in 59-85% yield.\",\"PeriodicalId\":22122,\"journal\":{\"name\":\"Sulfur Letters\",\"volume\":\"27 1\",\"pages\":\"87 - 93\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sulfur Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/02786110212862\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sulfur Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/02786110212862","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Functionally substituted 1,3-diethenyl [1,2- c ][1,3]pyrrolothiazoles from pyrrole-2-carbodithioates
The reaction of pyrrole-2-carbodithioates with methylenoactive nitriles and 2-benzoyl-1-bromoacetylene in the KOH-DMSO system leads to functionally substituted pyrrolothiazoles in 59-85% yield.