{"title":"4-苯基-2-亚甲基-1,3-二烯醇:合成与反应","authors":"Desikan Rajagopal, M. Lakshmikantham, M. Cava","doi":"10.1080/02786110212865","DOIUrl":null,"url":null,"abstract":"2-Methylene-4-phenyl-1,3-diselenole was synthesized. It was formylated on the exomethylene carbon in a Vilsmeier-Haack reaction; iodine-morpholine reagent converted it to the E/Z diphenyltetraselenafulvalene derivative.","PeriodicalId":22122,"journal":{"name":"Sulfur Letters","volume":"31 1","pages":"129 - 133"},"PeriodicalIF":0.0000,"publicationDate":"2002-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"4-Phenyl-2-methylene-1,3-diselenole: Synthesis and reactions\",\"authors\":\"Desikan Rajagopal, M. Lakshmikantham, M. Cava\",\"doi\":\"10.1080/02786110212865\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"2-Methylene-4-phenyl-1,3-diselenole was synthesized. It was formylated on the exomethylene carbon in a Vilsmeier-Haack reaction; iodine-morpholine reagent converted it to the E/Z diphenyltetraselenafulvalene derivative.\",\"PeriodicalId\":22122,\"journal\":{\"name\":\"Sulfur Letters\",\"volume\":\"31 1\",\"pages\":\"129 - 133\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sulfur Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/02786110212865\",\"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/10.1080/02786110212865","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
4-Phenyl-2-methylene-1,3-diselenole: Synthesis and reactions
2-Methylene-4-phenyl-1,3-diselenole was synthesized. It was formylated on the exomethylene carbon in a Vilsmeier-Haack reaction; iodine-morpholine reagent converted it to the E/Z diphenyltetraselenafulvalene derivative.
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