06 اردیبهشت 1403
داريوش صابري

داریوش صابری

مرتبه علمی: دانشیار
نشانی: دانشکده علوم و فناوری نانو و زیستی - گروه شیمی
تحصیلات: دکترای تخصصی / شیمی
تلفن: 07731222424
دانشکده: دانشکده علوم و فناوری نانو و زیستی

مشخصات پژوهش

عنوان
استری شدن اکسایشی بنزیل برمیدها: دسترسی مستقیم به بنزیل بنزوات ها
نوع پژوهش مقالات در همایش ها
کلیدواژه‌ها
oxidative-coupling, benzyl benzoates, benzyl bromides, metal-free, solvent-free
پژوهشگران داریوش صابری (نفر اول) ، هاجر هاشمی (نفر دوم)

چکیده

Selective to the C–O bond formation, the ester functionalities, particularly the benzylic esters, are common target because of their applications in synthetic organic and medicinal chemistry. Besides the traditional esterification reactions involving alcohols and acids (or their equivalents) several elegant protocols have been developed lately. Catalysts such as Ru, Rh, Ir, Pd ,V, and Cu have been employed for the oxidative coupling between aldehydes or the in situ generated aldehydes and alcohols for the synthesis of benzylic esters. Very recently Patel et al developed an elegant protocol based on the oxidative-coupling of alkyl benzenes under metal-free conditions for synthesis of benzylic esters although using an excess of alkynbenzene cuts the popularity of this method. In this line of research, we have found that the benzylic esters can be synthesized effectively via the oxidative-coupling of benzyl bromides under metal- and solvent-free conditions