Article ID Journal Published Year Pages File Type
1314344 Journal of Fluorine Chemistry 2010 6 Pages PDF
Abstract

The reactions of fluoroalkanesulfonyl azides with pyrrole and its derivatives were studied. The reaction proceeded smoothly under mild conditions to give the 3-(fluoroalkanesulfonamido) pyrroles in good yield. The electron donating groups on the pyrrole core accelerated the reaction, while the electron withdrawing groups decelerated it. All the products were fully characterized by spectrum methods, and one of the products was further confirmed by X-ray diffraction analysis. A possible reaction mechanism for these reactions was proposed.

Graphical abstractThe reactions of fluoroalkanesulfonyl azides with pyrrole and its derivatives were studied. The reaction proceeded smoothly under mild conditions to give the 3-(fluoroalkanesulfonamido) pyrroles in good yield. The electron donating groups on the pyrrole core accelerated the reaction, while the electron withdrawing groups decelerated it. All the products were fully characterized by spectrum methods, and one of the products was further confirmed by X-ray diffraction analysis. A possible reaction mechanism for these reactions was proposed.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
Authors
, , , ,