Advances in Organic Synthesis

Author(s): Teruo Umemoto

DOI: 10.2174/978160805198410602010159

N-Fluoropyridinium Salts, Synthesis and Fluorination Chemistry

Pp: 159-181 (23)

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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

Synthesis of N-fluoropyridinium salts and their synthetic application are discussed. Various types of stable N-fluoropyridinium salts are synthesized from unsubstituted and substituted pyridines and acids, their salts, silyl esters or Lewis acids by reaction with F2 diluted with N2. The N -fluoropyridinium salts are particularly useful as electrophilic fluorinating agents toward organic compounds in terms of easy handling and variability of fluorinating power and selectivity. This variability makes selective fluorination of a wide range of organic compounds differing in reactivity possible. Three classes of power- and selectivity-variable fluorinating agents, non-counterion-bound N-fluoropyridinium salt series, counterion-bound N-fluoropyridinium-sulfonate series, and dimeric N,N’- difluorobipyridinium salt series, were developed and successfully utilized for selective fluorinations of various substrates. As another synthetic application, a novel base-initiated reaction of N-fluoropyridinium salts producing α- fluoropyridines is discussed.

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