Abstract
One-pot reaction for the synthesis of symmetrical 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one is reported by condensing acenaphthenequinone and indoles in the presence of catalytic amount of amino-functionalized silica (SBA-Pr-NH2) under solvent-free conditions at 100 °C.
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We gratefully acknowledge the financial support from the Research Council of Alzahra University and the University of Tehran.
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Mohammadi Ziarani, G., Hajiabbasi, P. & Badiei, A. Application of SBA-Pr-NH2 as a nanoporous base silica catalyst in the development of 2,2-Bis(1H-indol-3-yl)acenaphthen-1(2H)-ones syntheses. J IRAN CHEM SOC 12, 1649–1654 (2015). https://doi.org/10.1007/s13738-015-0639-3
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DOI: https://doi.org/10.1007/s13738-015-0639-3