4.5 Review

Development of N-F fluorinating agents and their fluorinations: Historical perspective

期刊

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 17, 期 -, 页码 1752-1813

出版社

BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.17.123

关键词

N-F fluorinating agent; fluorination; fluorodiazoniabicyclo[2; 2; 2]octane salt; fluoropyridinium salt; fluorosulfonimide

资金

  1. National Institutes of Health [R01GM121660]

向作者/读者索取更多资源

This review covers the historical development of all N-F fluorinating agents developed to date, including various types of N-F compounds and their derivatives. It discusses the unique properties of fluorine that make fluorinated organic compounds attractive in research, and the usefulness of N-F agents due to their easy handling. The review also chronicles the synthesis, reactions, and relative fluorination power of each reagent from a historical perspective.
This review deals with the historical development of all N-F fluorinating agents developed so far. The unique properties of fluorine make fluorinated organic compounds attractive in many research areas and therefore fluorinating agents are important. N-F agents have proven useful by virtue of their easy handling. This reagent class includes many types of N-F compounds: perfluoro-N-fluo-ropiperidine, N-fluoro-2-pyridone, N-fluoro-N-alkylarenesulfonamides, N-fluoropyridinium salts and derivatives, N-fluoroquinu-clidium salts, N-fluoro-trifluoromethanesulfonimide, N-fluoro-sultams, N-fluoro-benzothiazole dioxides, N-fluoro-lactams, N-fluoro-o-benzenedisulfonimide, N-fluoro-benzenesulfonimide, 1-alkyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane salts, N-fluo-ropyridinium-2-sulfonate derivatives, 1-fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane salts, N-fluorodinitroimidazole, N-fluoro-trichloro-1,3,5-triazinium salt, N-F ethano-Troger's base derivatives, N-fluoro-methanesulfonimide, N-fluoro-N-arylarene-sulfonamides, bisN-F salts such as N,N'-difluorobipyridinium salts and N,N'-difluoro-1,4-diazoniabicyclo[2.2.2]octane salts, and their many derivatives and analogs, including chiral N-F reagents such as optically active N-fluoro-sultam derivatives, N-fluoro-alkaloid derivatives, DABCO-based N-F derivatives, and N-F binaphthyldisulfonimides. The synthesis and reactions of these reagents are described chronologically and the review also discusses the relative fluorination power of each reagent and their mech-anisms chronicling developments from a historical perspective.

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