{"title":"取自小苞草的克罗丹二萜类化合物","authors":"V. H. Verma, U. Mahmood, Bikram Singh","doi":"10.1080/10575630290020578","DOIUrl":null,"url":null,"abstract":"The whole plant of Ajuga bracteosa afforded five compounds including one new clerodane diterpenoid designated as Bracteonin-A ( 1 ) 6 f -acetoxy, 15 (R&S)-methoxy, 18-(4'-hydroxy, 3'- g -methyl, 3'- f -acetoxy, butyryloxy) neoclerodane. The other compounds identified were 14,15-dihydroajugapitin, 14-hydro-15-hydroxy ajugapitin, g -sitosterol, and stigmasterol. The structural elucidation was carried out by spectroscopic techniques.","PeriodicalId":18873,"journal":{"name":"Natural Product Letters","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2002-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"13","resultStr":"{\"title\":\"Clerodane Diterpenoids from Ajuga Bracteosa Wall\",\"authors\":\"V. H. Verma, U. Mahmood, Bikram Singh\",\"doi\":\"10.1080/10575630290020578\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The whole plant of Ajuga bracteosa afforded five compounds including one new clerodane diterpenoid designated as Bracteonin-A ( 1 ) 6 f -acetoxy, 15 (R&S)-methoxy, 18-(4'-hydroxy, 3'- g -methyl, 3'- f -acetoxy, butyryloxy) neoclerodane. The other compounds identified were 14,15-dihydroajugapitin, 14-hydro-15-hydroxy ajugapitin, g -sitosterol, and stigmasterol. The structural elucidation was carried out by spectroscopic techniques.\",\"PeriodicalId\":18873,\"journal\":{\"name\":\"Natural Product Letters\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Natural Product Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/10575630290020578\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/10575630290020578","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13
摘要
在小苞草属植物中发现了5个新化合物,包括一种新的氯烷二萜类化合物,命名为小苞草素-a (1) 6 f -乙酰氧基,15 (R&S)-甲氧基,18-(4'-羟基,3'- g -甲基,3'- f -乙酰氧基,丁基氧基)新氯烷。其他化合物鉴定为14,15-二氢合欢素、14-氢-15-羟基合欢素、g -谷甾醇和豆甾醇。用光谱技术对其结构进行了解析。
The whole plant of Ajuga bracteosa afforded five compounds including one new clerodane diterpenoid designated as Bracteonin-A ( 1 ) 6 f -acetoxy, 15 (R&S)-methoxy, 18-(4'-hydroxy, 3'- g -methyl, 3'- f -acetoxy, butyryloxy) neoclerodane. The other compounds identified were 14,15-dihydroajugapitin, 14-hydro-15-hydroxy ajugapitin, g -sitosterol, and stigmasterol. The structural elucidation was carried out by spectroscopic techniques.