Literature DB >> 15798975

The kinetic acidity of oligofluorobenzenes correlated with their gas phase deprotonation energies.

Manfred Schlosser1, Elena Marzi.   

Abstract

The relative reactivities of fluorobenzene, all di-, tri-, and tetrafluorobenzenes and pentafluorobenzene toward sec-butyllithium have been assessed in tetrahydrofuran at -100 degrees C. At this temperature no subsequent transmetalation reactions take place but those compromise the outcome of the competition experiments if the latter are conducted at -75 degrees C. The rates determined at -100 degrees C reflect the basicity differences between the naked (oligo)fluorophenyl anions to the extent of 10 %.

Entities:  

Year:  2005        PMID: 15798975     DOI: 10.1002/chem.200401094

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

Review 1.  Direct transition metal-catalyzed functionalization of heteroaromatic compounds.

Authors:  Ilya V Seregin; Vladimir Gevorgyan
Journal:  Chem Soc Rev       Date:  2007-03-05       Impact factor: 54.564

2.  Borylation of fluorinated arenes using the boron-centred nucleophile B(CN)32- - a unique entry to aryltricyanoborates.

Authors:  Johannes Landmann; Philipp T Hennig; Nikolai V Ignat'ev; Maik Finze
Journal:  Chem Sci       Date:  2017-06-26       Impact factor: 9.825

  2 in total

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