Synthesis of para-substituted bicyclo [2.2. 1] hept-5-en-2-ylmethyl benzoates

EG Mamedbeili, TG Kyazimova, ZM Nagiev…

Index: Mamedbeili; Kyazimova; Nagiev; Abdiev; Aliev Russian Journal of Organic Chemistry, 2009 , vol. 45, # 1 p. 74 - 77

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Abstract

Abstract para-Substituted bicyclo [2.2. 1] hept-5-en-2-ylmethyl benzoates were synthesized by the Diels-Alder reaction of cyclopentadiene with the corresponding para-substituted allyl benzoates, and optimal reaction conditions were found. The product structure was confirmed by independent synthesis and IR and 1 H NMR spectroscopy.

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