“…Some procedures require expensive and/or hazardous reagents such as, for example, perchloryl fluoride, others are difficult to repeat and/or are of limited applicability. Most of the papers published so far have been devoted to variously substituted fluorothiophenes [6][7][8][9][10][11][12][13][14][15][16][17], considerably fewer to pyrroles [16][17][18][19][20][21][22], and only a few to Journal of Fluorine Chemistry 124 (2003) [159][160][161][162][163][164][165][166][167][168] furans [16,17,23,24]. Though the methods of the synthesis of the fluoro-substituted heterocycles were not our primary goal, we had to check and/or modify the procedures chosen in order to synthesize the required model compounds.…”