{"title":"钯催化芳烃均偶联合成丁-1,3-二烯","authors":"Yanmei Wen, Jianying Xie, Chunmei Deng, Yulian Wu","doi":"10.1055/s-0034-1380749","DOIUrl":null,"url":null,"abstract":"Abstract A series of buta-1,3-dienes have been directly synthesized via a convenient palladium-catalyzed homodehydrogenation coupling reaction of aromatic alkenes under mild conditions. The homocoupling reaction enables a rapid synthesis of multisubstituted butadiene which shows typical aggregation-induced emission enhancement (AIEE) characteristics because it is practically not emissive in solution but emits blue fluorescence in aggregates.","PeriodicalId":22319,"journal":{"name":"Synlett","volume":"37 1","pages":"1755 - 1758"},"PeriodicalIF":1.7000,"publicationDate":"2015-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"10","resultStr":"{\"title\":\"Synthesis of Buta-1,3-dienes through Palladium-Catalyzed Homocoupling of Aromatic Alkenes\",\"authors\":\"Yanmei Wen, Jianying Xie, Chunmei Deng, Yulian Wu\",\"doi\":\"10.1055/s-0034-1380749\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract A series of buta-1,3-dienes have been directly synthesized via a convenient palladium-catalyzed homodehydrogenation coupling reaction of aromatic alkenes under mild conditions. The homocoupling reaction enables a rapid synthesis of multisubstituted butadiene which shows typical aggregation-induced emission enhancement (AIEE) characteristics because it is practically not emissive in solution but emits blue fluorescence in aggregates.\",\"PeriodicalId\":22319,\"journal\":{\"name\":\"Synlett\",\"volume\":\"37 1\",\"pages\":\"1755 - 1758\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2015-06-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synlett\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1055/s-0034-1380749\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synlett","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1055/s-0034-1380749","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Synthesis of Buta-1,3-dienes through Palladium-Catalyzed Homocoupling of Aromatic Alkenes
Abstract A series of buta-1,3-dienes have been directly synthesized via a convenient palladium-catalyzed homodehydrogenation coupling reaction of aromatic alkenes under mild conditions. The homocoupling reaction enables a rapid synthesis of multisubstituted butadiene which shows typical aggregation-induced emission enhancement (AIEE) characteristics because it is practically not emissive in solution but emits blue fluorescence in aggregates.
期刊介绍:
SYNLETT is an international journal reporting research results and current trends in chemical synthesis in short personalized reviews and preliminary communications. It covers all fields of scientific endeavor that involve organic synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines and offers the possibility to publish scientific primary data.