优化二硫真菌毒性:烃链长度的调整

Sulfur Letters Pub Date : 2002-01-01 DOI:10.1080/02786110213980

F. Baerlocher, M. Baerlocher, R. Langler, S. MacQuarrie, P. E. O'Connor

{"title":"优化二硫真菌毒性:烃链长度的调整","authors":"F. Baerlocher, M. Baerlocher, R. Langler, S. MacQuarrie, P. E. O'Connor","doi":"10.1080/02786110213980","DOIUrl":null,"url":null,"abstract":"Previously identified classes of antifungal disulfides are modified by extending alkyl substituents. Although, the principal focus is on f -sulfone disulfides, one nitrophenyl alkyl disulfide and a pair of f -ester disulfides were also prepared and examined. Optimum fungitoxicity is associated with structures which have seven to ten carbon atoms in the form of unbranched chains and/or phenyl rings.","PeriodicalId":22122,"journal":{"name":"Sulfur Letters","volume":"17 1","pages":"135 - 144"},"PeriodicalIF":0.0000,"publicationDate":"2002-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"13","resultStr":"{\"title\":\"Optimizing disulfide fungitoxicity: Adjustment of hydrocarbon chain length\",\"authors\":\"F. Baerlocher, M. Baerlocher, R. Langler, S. MacQuarrie, P. E. O'Connor\",\"doi\":\"10.1080/02786110213980\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Previously identified classes of antifungal disulfides are modified by extending alkyl substituents. Although, the principal focus is on f -sulfone disulfides, one nitrophenyl alkyl disulfide and a pair of f -ester disulfides were also prepared and examined. Optimum fungitoxicity is associated with structures which have seven to ten carbon atoms in the form of unbranched chains and/or phenyl rings.\",\"PeriodicalId\":22122,\"journal\":{\"name\":\"Sulfur Letters\",\"volume\":\"17 1\",\"pages\":\"135 - 144\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sulfur Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/02786110213980\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sulfur Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/02786110213980","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 13

摘要

以前鉴定的抗真菌类二硫化物是通过扩展烷基取代基来修饰的。虽然，主要的重点是磺砜二硫化物，硝基苯基烷基二硫化物和一对磺酯二硫化物也制备和测试。最佳的真菌毒性与具有7至10个碳原子的结构有关，其形式为无支链和/或苯环。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Optimizing disulfide fungitoxicity: Adjustment of hydrocarbon chain length

Previously identified classes of antifungal disulfides are modified by extending alkyl substituents. Although, the principal focus is on f -sulfone disulfides, one nitrophenyl alkyl disulfide and a pair of f -ester disulfides were also prepared and examined. Optimum fungitoxicity is associated with structures which have seven to ten carbon atoms in the form of unbranched chains and/or phenyl rings.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Sulfur Letters

自引率

0.00%

发文量