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Study of in situ generation of carbocationic system from trityl chloride (Ph3CCl) which efficiently catalyzed cross-aldol condensation reaction
Authors:Abdolkarim Zare  Maria Merajoddin  Alireza Hasaninejad  Ahmad Reza Moosavi-Zare  Vahid Khakyzadeh
Institution:1. Department of Chemistry, Payame Noor University, PO BOX 19395-3697, Tehran, Iran;2. Department of Chemistry, Faculty of Sciences, Persian Gulf University, 75169 Bushehr, Iran;3. Department of Chemistry, University of Sayyed Jamaleddin Asadabadi, 6541835583 Asadabad, Iran;4. Faculty of Chemistry, Bu-Ali Sina University, 6517838683 Hamedan, Iran
Abstract:Organocatalyst trityl chloride (Ph3CCl), by in situ formation of trityl carbocation with inherent instability, efficiently promotes the cross-aldol condensation reaction between cycloalkanones and arylaldehydes in solvent-free and homogeneous media to afford α,α′-bis(arylidene)cycloalkanones in high yields. Moreover, an attractive and plausible mechanism based on observations and the literature is proposed for the reaction.
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