1379764-13-2Relevant academic research and scientific papers
On the Vilsmeier formylation of N-aryl-substituted 2-aminothiophenes - A simple route to new thieno[2,3-b]quinolinium salts
Hartmann, Horst
, p. 356 - 370 (2013/09/24)
The Vilsmeier reaction of N-substituted 2-arylamino-thiophenes-5-carboxylic acid or their alkyl derivatives gives rise, depending on the substitution pattern at the thiophene moiety, to the formation of either N-substituted 2-arylamino-thiophene-5-carbaldehydes, corresponding imminium salt precursors, or novel thieno[2,3-b]quinolinium salts. These salts are highly reactive towards nucleophiles and can be easily transformed by reduction into the corresponding 4,9-dihydro derivatives. ARKAT-USA, Inc.
