全氟烷基的亲核加成

P. Beier, M. Zibinsky, G. Prakash
{"title":"全氟烷基的亲核加成","authors":"P. Beier, M. Zibinsky, G. Prakash","doi":"10.1002/0471264180.OR091.01","DOIUrl":null,"url":null,"abstract":"The trifluoromethyl and perfluoroalkyl functional groups possess significant thermal, chemical, and metabolic stability, as well as high lipophilicity and electronegativity. These physicochemical properties render fluorinated carbon residues indispensable in diverse applications, such as agrochemistry, drug design, and material chemistry. The generation and properties of nucleophilic perfluoroalkyl reagents as well as the scope and limitations of their additions to various electrophilic partners is described in this chapter. \n \n \nKeywords: \n \nfluorine; \ntrifluoromethyl; \nperfluoroalkyl; \nnucleophilic addition","PeriodicalId":19539,"journal":{"name":"Organic Reactions","volume":"61 1","pages":"1-492"},"PeriodicalIF":0.0000,"publicationDate":"2016-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":"{\"title\":\"Nucleophilic Additions of Perfluoroalkyl Groups\",\"authors\":\"P. Beier, M. Zibinsky, G. Prakash\",\"doi\":\"10.1002/0471264180.OR091.01\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The trifluoromethyl and perfluoroalkyl functional groups possess significant thermal, chemical, and metabolic stability, as well as high lipophilicity and electronegativity. These physicochemical properties render fluorinated carbon residues indispensable in diverse applications, such as agrochemistry, drug design, and material chemistry. The generation and properties of nucleophilic perfluoroalkyl reagents as well as the scope and limitations of their additions to various electrophilic partners is described in this chapter. \\n \\n \\nKeywords: \\n \\nfluorine; \\ntrifluoromethyl; \\nperfluoroalkyl; \\nnucleophilic addition\",\"PeriodicalId\":19539,\"journal\":{\"name\":\"Organic Reactions\",\"volume\":\"61 1\",\"pages\":\"1-492\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-12-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Reactions\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/0471264180.OR091.01\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Reactions","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/0471264180.OR091.01","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6

摘要

三氟甲基和全氟烷基官能团具有显著的热、化学和代谢稳定性,以及高亲脂性和电负性。这些物理化学性质使得氟化碳残留物在农业化学、药物设计和材料化学等各种应用中不可或缺。本章描述了亲核全氟烷基试剂的生成和性质,以及它们添加到各种亲电伙伴中的范围和限制。关键词:氟;trifluoromethyl;全氟烃基;亲核加成
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
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Nucleophilic Additions of Perfluoroalkyl Groups
The trifluoromethyl and perfluoroalkyl functional groups possess significant thermal, chemical, and metabolic stability, as well as high lipophilicity and electronegativity. These physicochemical properties render fluorinated carbon residues indispensable in diverse applications, such as agrochemistry, drug design, and material chemistry. The generation and properties of nucleophilic perfluoroalkyl reagents as well as the scope and limitations of their additions to various electrophilic partners is described in this chapter. Keywords: fluorine; trifluoromethyl; perfluoroalkyl; nucleophilic addition
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
CiteScore
4.40
自引率
0.00%
发文量
0
期刊最新文献
Cyclization Reactions of Nitrogen‐Centered Radicals Hauser–Kraus, Sammes, Staunton–Weinreb, and Tamura Annulations Enantioselective Hydroformylation Alkene Cross‐Metathesis Reactions The Catalytic Enantioselective Stetter Reaction
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1