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Molbank 2006, 2006(2), M474; doi:10.3390/M474
Short Note


1,* , 2, 3, 3, 1, 1 and 1
Received: 30 January 2006 / Accepted: 9 March 2006 / Published: 10 March 2006
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Abstract: Synthesis of 5,5’-biindole was carried out by the Madelung indole reaction. Under strong basic conditions and high temperatures (350 ºC), N,N’-bis-formyl-o-tolidine underwent cyclization to produce high amounts of the dimeric indole. Full and unambiguous assignments of all 1H- and 13C-NMR resonances of indole and 5,5’-biindole in DMSO-d6 are also reported.
Keywords: Indoloquinolizine; Antitumor activity; Teuber’s reaction; Indole synthesis; 1H-NMR; 13C-NMR Indoloquinolizine; Antitumor activity; Teuber’s reaction; Indole synthesis; 1H-NMR; 13C-NMR
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MDPI and ACS Style

Quintanilla-Licea, R.; Colunga-Valladares, J.F.; Caballero-Quintero, A.; Waksman, N.; Gomez-Flores, R.; Rodríguez-Padilla, C.; Tamez-Guerra, R. 5,5’-Biindole. Molbank 2006, 2006, M474.

AMA Style

Quintanilla-Licea R, Colunga-Valladares JF, Caballero-Quintero A, Waksman N, Gomez-Flores R, Rodríguez-Padilla C, Tamez-Guerra R. 5,5’-Biindole. Molbank. 2006; 2006(2):M474.

Chicago/Turabian Style

Quintanilla-Licea, Ramiro; Colunga-Valladares, Juan F.; Caballero-Quintero, Adolfo; Waksman, Noemí; Gomez-Flores, Ricardo; Rodríguez-Padilla, Cristina; Tamez-Guerra, Reyes. 2006. "5,5’-Biindole." Molbank 2006, no. 2: M474.

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