N-Fluoropyridinium Salts, Synthesis and Fluorination Chemistry
- By Teruo Umemoto
- Source: Advances in Organic Synthesis: Volume 2 , pp 159-181
- Publication Date: January 2006
- Language: English
N-Fluoropyridinium Salts, Synthesis and Fluorination Chemistry, Page 1 of 1
< Previous page | Next page > /docserver/preview/fulltext/9781608051984/chapter-5-1.gif
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.
-
From This Site
/content/books/9781608051984.chapter-5dcterms_subject,pub_keyword-contentType:Journal -contentType:Figure -contentType:Table -contentType:SupplementaryData105