{"title":"5-氯甲基-2-羟基苯甲醛衍生的水杨醛-合成与反应","authors":"Gheorghe Roman","doi":"10.23939/chcht17.03.532","DOIUrl":null,"url":null,"abstract":"A series of salicylaldehydes have been prepared through the replacement of the easily leaving chlorine atom in 5-chloromethyl-2-hydroxybenzaldehyde with various O-, S- or N-nucleophiles. The involvement of a few of these salicylaldehydes in the synthesis of heterocycles such as benzofuran or coumarin, or as substrate in the Petasis borono-Mannich reaction has been explored.","PeriodicalId":9762,"journal":{"name":"Chemistry and Chemical Technology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Salicylaldehydes Derived from 5-Chloromethyl-2-hydroxybenzaldehyde – Synthesis and Reactions\",\"authors\":\"Gheorghe Roman\",\"doi\":\"10.23939/chcht17.03.532\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A series of salicylaldehydes have been prepared through the replacement of the easily leaving chlorine atom in 5-chloromethyl-2-hydroxybenzaldehyde with various O-, S- or N-nucleophiles. The involvement of a few of these salicylaldehydes in the synthesis of heterocycles such as benzofuran or coumarin, or as substrate in the Petasis borono-Mannich reaction has been explored.\",\"PeriodicalId\":9762,\"journal\":{\"name\":\"Chemistry and Chemical Technology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-09-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry and Chemical Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.23939/chcht17.03.532\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry and Chemical Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.23939/chcht17.03.532","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Salicylaldehydes Derived from 5-Chloromethyl-2-hydroxybenzaldehyde – Synthesis and Reactions
A series of salicylaldehydes have been prepared through the replacement of the easily leaving chlorine atom in 5-chloromethyl-2-hydroxybenzaldehyde with various O-, S- or N-nucleophiles. The involvement of a few of these salicylaldehydes in the synthesis of heterocycles such as benzofuran or coumarin, or as substrate in the Petasis borono-Mannich reaction has been explored.
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