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Information Journal Paper

Title

L-PROLINE CATALYZED SYNTHESIS OF BETTI BASES AND BISCOUMARIN DERIVATIVES

Pages

  149-153

Abstract

 The direct three component modified Mannich reaction via condensation of aldehydes, 2-naphthol or 2, 7-naphthalendiol and piperidine to generate BETTI BASEs has been carried out over L-PROLINE (20 mol%) with high efficiency under solvent-free conditions at 70oC. Also, the reaction of aromatic aldehyde and 4-hydroxycoumarin in the presence of L-PROLINE (20 mol%) in the ethanol under reflux conditions, lead to BISCOUMARIN derivatives.

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  • Cite

    APA: Copy

    ZAHIRI, SAMANEH, MOKHTARI, MASOUD, & TORABI, MOGHARAB. (2015). L-PROLINE CATALYZED SYNTHESIS OF BETTI BASES AND BISCOUMARIN DERIVATIVES. IRANIAN JOURNAL OF CATALYSIS, 5(2), 149-153. SID. https://sid.ir/paper/680336/en

    Vancouver: Copy

    ZAHIRI SAMANEH, MOKHTARI MASOUD, TORABI MOGHARAB. L-PROLINE CATALYZED SYNTHESIS OF BETTI BASES AND BISCOUMARIN DERIVATIVES. IRANIAN JOURNAL OF CATALYSIS[Internet]. 2015;5(2):149-153. Available from: https://sid.ir/paper/680336/en

    IEEE: Copy

    SAMANEH ZAHIRI, MASOUD MOKHTARI, and MOGHARAB TORABI, “L-PROLINE CATALYZED SYNTHESIS OF BETTI BASES AND BISCOUMARIN DERIVATIVES,” IRANIAN JOURNAL OF CATALYSIS, vol. 5, no. 2, pp. 149–153, 2015, [Online]. Available: https://sid.ir/paper/680336/en

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