V. Potapov, S. Amosova, I. V. Doron'kina, R. Glass
{"title":"(Z)-1,2-二(苄基硒)-乙烯的意外反应:1,4-二硒素的生成","authors":"V. Potapov, S. Amosova, I. V. Doron'kina, R. Glass","doi":"10.1080/0278611031000138018","DOIUrl":null,"url":null,"abstract":"Heating (Z)-1,2-bis(benzylseleno)ethene at 140–180 °C leads to 1,4-diselenin (79% yield) and dibenzyl selenide. This unusual reaction represents a convenient method for preparing 1,4-diselenin.","PeriodicalId":22122,"journal":{"name":"Sulfur Letters","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2003-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Unexpected reaction of (Z)-1,2-bis(benzylseleno)-ethene: The formation of 1,4-diselenin\",\"authors\":\"V. Potapov, S. Amosova, I. V. Doron'kina, R. Glass\",\"doi\":\"10.1080/0278611031000138018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Heating (Z)-1,2-bis(benzylseleno)ethene at 140–180 °C leads to 1,4-diselenin (79% yield) and dibenzyl selenide. This unusual reaction represents a convenient method for preparing 1,4-diselenin.\",\"PeriodicalId\":22122,\"journal\":{\"name\":\"Sulfur Letters\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sulfur Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/0278611031000138018\",\"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/10.1080/0278611031000138018","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Unexpected reaction of (Z)-1,2-bis(benzylseleno)-ethene: The formation of 1,4-diselenin
Heating (Z)-1,2-bis(benzylseleno)ethene at 140–180 °C leads to 1,4-diselenin (79% yield) and dibenzyl selenide. This unusual reaction represents a convenient method for preparing 1,4-diselenin.