{"title":"黄斑天牛雌性接触性信息素21-甲基-8-五三康内烯四种可能立体异构体的合成","authors":"Eiichiro Fukusaki , Shiro Satoda , Hiroyuki Yuasa , Shuji Senda , Tetsuo Omata , Midori Fukaya , Sadao Wakamura","doi":"10.1016/S0922-338X(97)80366-2","DOIUrl":null,"url":null,"abstract":"<div><p>The synthesis of the four possible stereoisomers of 21-methyl-8-pentatriacontene, the (<em>R</em>)- and (<em>S</em>)-enantiomers of both (<em>Z</em>)- and (<em>E</em>)-geometrical isomers, was achieved by starting from the enantiomers of 3-hydroxy-2-methylpropionate, 1-nonyne and 1,10-decandiol to evaluate the response of the male yellow-spotted longicorn beetle, <em>Psacothea hilaris</em>.</p></div>","PeriodicalId":15696,"journal":{"name":"Journal of Fermentation and Bioengineering","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1998-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0922-338X(97)80366-2","citationCount":"6","resultStr":"{\"title\":\"Synthesis of the four possible stereoisomers of 21-methyl-8-pentatriacontene, the female contact sex pheromone of the yellow-spotted longicorn beetle, Psacothea hilaris\",\"authors\":\"Eiichiro Fukusaki , Shiro Satoda , Hiroyuki Yuasa , Shuji Senda , Tetsuo Omata , Midori Fukaya , Sadao Wakamura\",\"doi\":\"10.1016/S0922-338X(97)80366-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The synthesis of the four possible stereoisomers of 21-methyl-8-pentatriacontene, the (<em>R</em>)- and (<em>S</em>)-enantiomers of both (<em>Z</em>)- and (<em>E</em>)-geometrical isomers, was achieved by starting from the enantiomers of 3-hydroxy-2-methylpropionate, 1-nonyne and 1,10-decandiol to evaluate the response of the male yellow-spotted longicorn beetle, <em>Psacothea hilaris</em>.</p></div>\",\"PeriodicalId\":15696,\"journal\":{\"name\":\"Journal of Fermentation and Bioengineering\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1998-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0922-338X(97)80366-2\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Fermentation and Bioengineering\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0922338X97803662\",\"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 Fermentation and Bioengineering","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0922338X97803662","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis of the four possible stereoisomers of 21-methyl-8-pentatriacontene, the female contact sex pheromone of the yellow-spotted longicorn beetle, Psacothea hilaris
The synthesis of the four possible stereoisomers of 21-methyl-8-pentatriacontene, the (R)- and (S)-enantiomers of both (Z)- and (E)-geometrical isomers, was achieved by starting from the enantiomers of 3-hydroxy-2-methylpropionate, 1-nonyne and 1,10-decandiol to evaluate the response of the male yellow-spotted longicorn beetle, Psacothea hilaris.