{"title":"尼日利亚多汁的大戟。二、博氏乳杆菌(E.poisonii Pax)胶乳的脂族二萜酯。和E.unispina N.E.Br。","authors":"R J Schmidt, F J Evans","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Methanol-preserved latices of E. poisonii and E. unispina were examined for irritant principles. Six esters of the parent diterpene 12-deoxyphorbol were identified by spectroscopic and chemical methods. Three were the aliphatic esters 12-deoxyphorbol-13-(2-methyl-butyrate), 12-deoxyphorbol-13-angelate and 12-deoxyphorbol-13-isobutyrate, and a further three compounds were the 20-acetyl equivalents. Isobutyrate esters were absent from the latex of E. unispina, an observation of possible value in the identification of these two similar species.</p>","PeriodicalId":18256,"journal":{"name":"Lloydia","volume":"40 3","pages":"225-9"},"PeriodicalIF":0.0000,"publicationDate":"1977-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The succulent Euphorbias of Nigeria. II. aliphatic diterpene esters of the latices of E. poisonii Pax. and E. unispina N.E. Br.\",\"authors\":\"R J Schmidt, F J Evans\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Methanol-preserved latices of E. poisonii and E. unispina were examined for irritant principles. Six esters of the parent diterpene 12-deoxyphorbol were identified by spectroscopic and chemical methods. Three were the aliphatic esters 12-deoxyphorbol-13-(2-methyl-butyrate), 12-deoxyphorbol-13-angelate and 12-deoxyphorbol-13-isobutyrate, and a further three compounds were the 20-acetyl equivalents. Isobutyrate esters were absent from the latex of E. unispina, an observation of possible value in the identification of these two similar species.</p>\",\"PeriodicalId\":18256,\"journal\":{\"name\":\"Lloydia\",\"volume\":\"40 3\",\"pages\":\"225-9\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1977-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Lloydia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lloydia","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The succulent Euphorbias of Nigeria. II. aliphatic diterpene esters of the latices of E. poisonii Pax. and E. unispina N.E. Br.
Methanol-preserved latices of E. poisonii and E. unispina were examined for irritant principles. Six esters of the parent diterpene 12-deoxyphorbol were identified by spectroscopic and chemical methods. Three were the aliphatic esters 12-deoxyphorbol-13-(2-methyl-butyrate), 12-deoxyphorbol-13-angelate and 12-deoxyphorbol-13-isobutyrate, and a further three compounds were the 20-acetyl equivalents. Isobutyrate esters were absent from the latex of E. unispina, an observation of possible value in the identification of these two similar species.