Abstract
An efficient nucleophilic addition reaction of indole derivatives with various synthesized azo-linked aldehydes to afford novel derivatives of diindolylmethane was carried out using a catalytic amount of L-proline, K10 and nano- Fe3O4 in aqeous media.
Keywords: Diindolylmethanes, indole, K10, L-proline, nano-Fe3O4, polymer, molecular iodine, indium, chloride, chloride
Letters in Organic Chemistry
Title:Comparative Study for the Aqeous Synthesis of New Generation of Diindolylmethanes Using L-Proline, K10 and Nano-Fe3O4 under Ultrasound Irradiation
Volume: 9 Issue: 5
Author(s): Mohammad Nikpassand, Leila Zare and Mohammad R. Mousavi
Affiliation:
Keywords: Diindolylmethanes, indole, K10, L-proline, nano-Fe3O4, polymer, molecular iodine, indium, chloride, chloride
Abstract: An efficient nucleophilic addition reaction of indole derivatives with various synthesized azo-linked aldehydes to afford novel derivatives of diindolylmethane was carried out using a catalytic amount of L-proline, K10 and nano- Fe3O4 in aqeous media.
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Cite this article as:
Nikpassand Mohammad, Zare Leila and R. Mousavi Mohammad, Comparative Study for the Aqeous Synthesis of New Generation of Diindolylmethanes Using L-Proline, K10 and Nano-Fe3O4 under Ultrasound Irradiation, Letters in Organic Chemistry 2012; 9 (5) . https://dx.doi.org/10.2174/157017812801264719
DOI https://dx.doi.org/10.2174/157017812801264719 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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