{"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}
引用次数: 2
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.
京公网安备 11010802042870号
京ICP备2023020795号-1
分享
求助内容：
应助结果提醒方式：
扫码关注我们
