A K Ganguly, V M Girijavallabhan, G H Miller, O Z Sarre
{"title":"抗菌药物的化学修饰。","authors":"A K Ganguly, V M Girijavallabhan, G H Miller, O Z Sarre","doi":"10.7164/antibiotics.35.561","DOIUrl":null,"url":null,"abstract":"<p><p>Novel antibiotic everninomicin D is chemically transformed into new biologically active derivatives. Reactions of a nitro group attached to a tertiary carbon center have been investigated. Synthesis and reactions of hydroxylaminoeverninomicin D, aminoeverninomicin D and their derivatives have been discussed.</p>","PeriodicalId":501839,"journal":{"name":"The Journal of Antibiotics","volume":" ","pages":"561-70"},"PeriodicalIF":0.0000,"publicationDate":"1982-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.7164/antibiotics.35.561","citationCount":"26","resultStr":"{\"title\":\"Chemical modification of everninomicins.\",\"authors\":\"A K Ganguly, V M Girijavallabhan, G H Miller, O Z Sarre\",\"doi\":\"10.7164/antibiotics.35.561\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Novel antibiotic everninomicin D is chemically transformed into new biologically active derivatives. Reactions of a nitro group attached to a tertiary carbon center have been investigated. Synthesis and reactions of hydroxylaminoeverninomicin D, aminoeverninomicin D and their derivatives have been discussed.</p>\",\"PeriodicalId\":501839,\"journal\":{\"name\":\"The Journal of Antibiotics\",\"volume\":\" \",\"pages\":\"561-70\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1982-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.7164/antibiotics.35.561\",\"citationCount\":\"26\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Antibiotics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.7164/antibiotics.35.561\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Antibiotics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.7164/antibiotics.35.561","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Novel antibiotic everninomicin D is chemically transformed into new biologically active derivatives. Reactions of a nitro group attached to a tertiary carbon center have been investigated. Synthesis and reactions of hydroxylaminoeverninomicin D, aminoeverninomicin D and their derivatives have been discussed.
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