Pyrrolo[2,3-c]quinolines and pyrrolo[3,4-c]quinolines - Synthesis and investigation of lipoxygenase inhibition
The Paal-Knorr synthesis of the cyclic hemiketonacetal 4 yields the pyrrole-2,4-dicarboxylic acid diesters 1c and 7 via the cyclic hemiaminals 5 and 6; while the pyrrole-2-carboxylic acid ester 9 is formed from the 1,4-diketon 10. Under reducing condition
Goerlitzer,Fabian,Frohberg,Drutkowski
p. 243 - 247
(2007/10/03)
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