Advances in Organic Synthesis

Author(s): Stojan Stavber and Marko Zupan

DOI: 10.2174/978160805198410602010213

N-Fluoro-1,4-Diazoniabicyclo[2.2.2]octane Dication Salts; Efficient Fluorinating Agents and Functionalization Mediators for Organic Compounds

Pp: 213-268 (56)

Buy Chapters

* (Excluding Mailing and Handling)

  • * (Excluding Mailing and Handling)

Abstract

SHS investigation development is considered from the geographical and historical viewpoint. 3 stages are described. Within Stage 1 the work was carried out in the Department of the Institute of Chemical Physics in Chernogolovka where the scientific discovery had been made. At Stage 2 the interest to SHS arose in different cities and towns of the former USSR. Within Stage 3 SHS entered the international scene. Now SHS processes and products are being studied in more than 50 countries.

Abstract

Fluorination of organic compounds using the most representative reagents from the group of N-fluoro-1,4-diazoniabicyclo[2.2.2]octane dication salts is reviewed. Data dealing with selective fluorofunctionalization of aromatics, alkenes, alkynes, saturated hydrocarbons, organometallics, and organic molecules bearing nitrogen, sulfur, phosphorus, silicon or carbonyl containing functional groups with SelectfluorTM F-TEDA-BF4 1 (1-chloromethyl- 4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetra-fluoroborate)), Accufluor™ NFTh 2 (1-fluoro-4-hydroxy-1,4-diazoniabicyclo [2.2.2]octane bis(tetrafluoroborate)) or bis(NF)-TEDA-BF4 3 (1,4-difluoro-1,4-diazoniabicyclo[ 2.2.2]octane bis (tetrafluoroborate)) are systematically collected and comparatively evaluated. Fluorination of potentially bioactive organic molecules (steroids, pyrimidine bases, glycols …) with the above mentioned reagents is particularly emphasized. Functionalization of organic compounds mediated by Selectfluor™ F-TEDA-BF4 is briefly reviewed.

Recommended Chapters

We recommend

Favorable 70-S: Investigation Branching Arrow

Authors:Bentham Science Books