{"title":"一种简便的吲哚酮制备方法","authors":"P. H. Lacy, D. C. Smith","doi":"10.1039/J39710000041","DOIUrl":null,"url":null,"abstract":"Indenone is made in two steps from indane-1,3-dione, and a by-product is characterised by conversion to s-dibenzofulvalene. Indenone undergoes acid-catalysed addition reactions, and all its six protons have magnetic resonance at higher field than expected.","PeriodicalId":17245,"journal":{"name":"Journal of The Chemical Society C: Organic","volume":"20 1","pages":"41-43"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"A convenient preparation of indenone\",\"authors\":\"P. H. Lacy, D. C. Smith\",\"doi\":\"10.1039/J39710000041\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Indenone is made in two steps from indane-1,3-dione, and a by-product is characterised by conversion to s-dibenzofulvalene. Indenone undergoes acid-catalysed addition reactions, and all its six protons have magnetic resonance at higher field than expected.\",\"PeriodicalId\":17245,\"journal\":{\"name\":\"Journal of The Chemical Society C: Organic\",\"volume\":\"20 1\",\"pages\":\"41-43\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society C: Organic\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/J39710000041\",\"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 C: Organic","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J39710000041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Indenone is made in two steps from indane-1,3-dione, and a by-product is characterised by conversion to s-dibenzofulvalene. Indenone undergoes acid-catalysed addition reactions, and all its six protons have magnetic resonance at higher field than expected.
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