TY - JOUR
T1 - Synthesis and chemiluminescent activity of 8,9-dihydrobenzo[g]pyridazino[4,5-b]indole-7,10(11h)-diones
AU - Kurumi, Masateru
AU - Sasaki, Kenji
AU - Takata, Hiroko
AU - Nakayama, Taiji
PY - 2001/1/1
Y1 - 2001/1/1
N2 - Substituted and unsubstituted naphthylamines were transformed into the corresponding triazole derivatives, which were converted to dimethyl 1H-benz[g]indole-2,3-dicarboxylates by photocyclization. The reaction of the diesters with hydrazine hydrate gave the corresponding 8,9-dihydrobenzo[g]pyridazino[4,5-b]indole-7,10(11H)-diones (5). One of compounds 5 was found to have chemiluminescent activity similar to luminol.
AB - Substituted and unsubstituted naphthylamines were transformed into the corresponding triazole derivatives, which were converted to dimethyl 1H-benz[g]indole-2,3-dicarboxylates by photocyclization. The reaction of the diesters with hydrazine hydrate gave the corresponding 8,9-dihydrobenzo[g]pyridazino[4,5-b]indole-7,10(11H)-diones (5). One of compounds 5 was found to have chemiluminescent activity similar to luminol.
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U2 - 10.1002/jhet.5570380313
DO - 10.1002/jhet.5570380313
M3 - Article
AN - SCOPUS:0034937961
SN - 0022-152X
VL - 38
SP - 629
EP - 632
JO - Journal of Heterocyclic Chemistry
JF - Journal of Heterocyclic Chemistry
IS - 3
ER -