{"title":"rac-2 - {3 - (1 - (Acet-yloxy) eth-yl) 2, 2-di-methyl-cyclobut-yl}醋酸。","authors":"Dieter Schollmeyer , Paul Jirsch , Heiner Detert","doi":"10.1107/S2414314624011441","DOIUrl":null,"url":null,"abstract":"<div><div>The title compound was prepared from α-pinene in three steps. The ester and acid moieties are <em>cis</em> on the slightly folded cyclobutane ring. In the crystal, carboxylic acid bound dimers form layers parallel to (202).</div></div><div><div>The title compound, C<sub>12</sub>H<sub>20</sub>O<sub>4</sub>, was prepared from α-pinene in three steps. The ester and acid moieties are <em>cis</em> on the slightly folded cyclobutane ring. In the crystal, carboxylic acid bound dimers form layers parallel to (202).<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (180KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":94324,"journal":{"name":"IUCrData","volume":"9 12","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11701758/pdf/","citationCount":"0","resultStr":"{\"title\":\"rac-2-{3-[1-(Acetyloxy)ethyl]-2,2-dimethylcyclobutyl}acetic acid\",\"authors\":\"Dieter Schollmeyer , Paul Jirsch , Heiner Detert\",\"doi\":\"10.1107/S2414314624011441\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The title compound was prepared from α-pinene in three steps. The ester and acid moieties are <em>cis</em> on the slightly folded cyclobutane ring. In the crystal, carboxylic acid bound dimers form layers parallel to (202).</div></div><div><div>The title compound, C<sub>12</sub>H<sub>20</sub>O<sub>4</sub>, was prepared from α-pinene in three steps. The ester and acid moieties are <em>cis</em> on the slightly folded cyclobutane ring. In the crystal, carboxylic acid bound dimers form layers parallel to (202).<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (180KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>\",\"PeriodicalId\":94324,\"journal\":{\"name\":\"IUCrData\",\"volume\":\"9 12\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11701758/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IUCrData\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2414314624001202\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IUCrData","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2414314624001202","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The title compound was prepared from α-pinene in three steps. The ester and acid moieties are cis on the slightly folded cyclobutane ring. In the crystal, carboxylic acid bound dimers form layers parallel to (202).
The title compound, C12H20O4, was prepared from α-pinene in three steps. The ester and acid moieties are cis on the slightly folded cyclobutane ring. In the crystal, carboxylic acid bound dimers form layers parallel to (202).
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