{"title":"丁香酚1异构体的合成","authors":"G. Brauer, Richard W. Morris, Willard B. Howe","doi":"10.6028/jres.067A.026","DOIUrl":null,"url":null,"abstract":"In connection with an investigation of the correlation between structure and reactivity of eugenol isomers, o-eugenol, 3-allyl-2-methoxyphenol and chavibetol were synthesized. A five-step synthesis was found to be most suitable for the preparation of 3-allyl-2-methoxyphenol. An improved separation of chavibetol from eugenol was achieved by gas chromatography.","PeriodicalId":94340,"journal":{"name":"Journal of research of the National Bureau of Standards. Section A, Physics and chemistry","volume":"54 1","pages":"253 - 257"},"PeriodicalIF":0.0000,"publicationDate":"1963-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Synthesis of Isomers of Eugenol1\",\"authors\":\"G. Brauer, Richard W. Morris, Willard B. Howe\",\"doi\":\"10.6028/jres.067A.026\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In connection with an investigation of the correlation between structure and reactivity of eugenol isomers, o-eugenol, 3-allyl-2-methoxyphenol and chavibetol were synthesized. A five-step synthesis was found to be most suitable for the preparation of 3-allyl-2-methoxyphenol. An improved separation of chavibetol from eugenol was achieved by gas chromatography.\",\"PeriodicalId\":94340,\"journal\":{\"name\":\"Journal of research of the National Bureau of Standards. Section A, Physics and chemistry\",\"volume\":\"54 1\",\"pages\":\"253 - 257\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1963-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of research of the National Bureau of Standards. Section A, Physics and chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.6028/jres.067A.026\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of research of the National Bureau of Standards. Section A, Physics and chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.6028/jres.067A.026","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
In connection with an investigation of the correlation between structure and reactivity of eugenol isomers, o-eugenol, 3-allyl-2-methoxyphenol and chavibetol were synthesized. A five-step synthesis was found to be most suitable for the preparation of 3-allyl-2-methoxyphenol. An improved separation of chavibetol from eugenol was achieved by gas chromatography.