{"title":"(±)-芬屈酮的合成,(+)-芬屈酮和(+)-顺式-2,2,5-三甲基-3-乙烯基环戊酮的合成,(-)-反式-4-酮的光异构体","authors":"P. Boyle, W. Cocker, D. H. Grayson, P. Shannon","doi":"10.1039/C29710000395","DOIUrl":null,"url":null,"abstract":"(+)-cis-3-(2-Hydroxyethyl)-2,2,5-trimethyl-cyclopentanone and its racemic form are synthesised from (+)-α-2,3-epoxypinane or (–)-trans-pinocarveol, and (±)-2,2,5-trimethyl-1-oxocyclopentane-3-carboxylic acid, respectively; treatment with base of the chloroketone, derived from the (+)-hydroxyketone, affords (+)-fenchone, while pyrolysis of the (+)-acetoxyketone gives (+)-cis-2,2,5-trimethyl-3-vinylcyclopentanone, the latter and its trans-isomer being photo-products of (–)-trans-and (–)-cis-caran-4-one, respectively.","PeriodicalId":17278,"journal":{"name":"Journal of The Chemical Society D: Chemical Communications","volume":"174 1","pages":"395-396"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Total synthesis of (±)-fenchone, a synthesis of (+)-fenchone and of (+)-cis-2,2,5-trimethyl-3-vinylcyclopentanone, a photoisomer of (–)-trans-caran-4-one\",\"authors\":\"P. Boyle, W. Cocker, D. H. Grayson, P. Shannon\",\"doi\":\"10.1039/C29710000395\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"(+)-cis-3-(2-Hydroxyethyl)-2,2,5-trimethyl-cyclopentanone and its racemic form are synthesised from (+)-α-2,3-epoxypinane or (–)-trans-pinocarveol, and (±)-2,2,5-trimethyl-1-oxocyclopentane-3-carboxylic acid, respectively; treatment with base of the chloroketone, derived from the (+)-hydroxyketone, affords (+)-fenchone, while pyrolysis of the (+)-acetoxyketone gives (+)-cis-2,2,5-trimethyl-3-vinylcyclopentanone, the latter and its trans-isomer being photo-products of (–)-trans-and (–)-cis-caran-4-one, respectively.\",\"PeriodicalId\":17278,\"journal\":{\"name\":\"Journal of The Chemical Society D: Chemical Communications\",\"volume\":\"174 1\",\"pages\":\"395-396\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society D: Chemical Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/C29710000395\",\"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 The Chemical Society D: Chemical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/C29710000395","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Total synthesis of (±)-fenchone, a synthesis of (+)-fenchone and of (+)-cis-2,2,5-trimethyl-3-vinylcyclopentanone, a photoisomer of (–)-trans-caran-4-one
(+)-cis-3-(2-Hydroxyethyl)-2,2,5-trimethyl-cyclopentanone and its racemic form are synthesised from (+)-α-2,3-epoxypinane or (–)-trans-pinocarveol, and (±)-2,2,5-trimethyl-1-oxocyclopentane-3-carboxylic acid, respectively; treatment with base of the chloroketone, derived from the (+)-hydroxyketone, affords (+)-fenchone, while pyrolysis of the (+)-acetoxyketone gives (+)-cis-2,2,5-trimethyl-3-vinylcyclopentanone, the latter and its trans-isomer being photo-products of (–)-trans-and (–)-cis-caran-4-one, respectively.