Double functionalization of Pyridine as a substance with abundant biological properties
Mehran Ghasemi - Azizollah Habibi
Mehran Ghasemi - Azizollah Habibi
Faculty of Chemistry, Kharazmi University, No. 43. Mofateh Street, Enghelab Ave., 15719-14911 Tehran, Iran - Faculty of Chemistry, Kharazmi University, No. 43. Mofateh Street, Enghelab Ave., 15719-14911 Tehran, Iran
زبان مقاله : انگلیسی |
تعداد صفحات مقاله : 1 صفحه |
نوع مقاله : چکیده |
ISC کد مقاله در : ISC4026_524533
چکیده
pyridine scaffold one of the most important class of heterocycles, is ubiquitous in a wide variety of organisms and biologically active structures. [1] Many drugs currently on the market contain pyridine core nucleus. Due to the biological properties of pyridine, there have been many reports of the functionalization of these compounds in the last decade. [2] One of the attractive ways to functionalization of different compounds is to use Catellani's strategy. [3] In this approach it is possible to functionalization two positions in a one pot. In this work, this strategy was used to double functionalization of pyridine compounds. 2-iodopyridine derivatives have been used as a source of pyridine. The reaction involves the cyanation of position 2 and the alkylation of position 3 of pyridine. Thus, the process involves coupling to position 2, and C-H activation at position 3. The reaction is carried out in the presence of palladium acetate as a catalyst and the triphenylphosphine as a ligand, and Zn(CN)2 as the cyanide source. The features of this work include the formation of palladacycle as an intermediate for C-H activation of 3-position of pyridine. So, a practical method was proposed for the double functionalization of pyridine in which palladium acetate was used for C-H activation and Zn(CN)2 was used as a cheap and available source for pyridine cyanation. Although norbornene not present in the finished product, its role in the formation of palladacycle and C-H activation of 3-position of pyridine is unavoidable.کليدواژه ها
Pyridine, cyanation, palladium, catellani reactionنحوه استناد به مقاله
در صورتی که می خواهید در اثر پژوهشی خود به این مقاله ارجاع دهید، به سادگی می توانید از عبارت زیر در بخش منابع و مراجع استفاده نمایید:Ghasemi , Mehran , 1398 , Double functionalization of Pyridine as a substance with abundant biological properties , دومین کنفرانس ملی کاتالیست انجمن شیمی ایران
انتشار دهنده
محل انتشار : دومین کنفرانس ملی کاتالیست انجمن شیمی ایرانمشخصات برگزارکننده همایش : دانشگاه خوارزمي
تعداد مقالات : 215
کد اختصاصی :
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