An efficient synthesis of 2-aminopyrroles from enaminone–amidine adduct and phenacyl/benzyl/heteroalkyl-halides

التفاصيل البيبلوغرافية
العنوان: An efficient synthesis of 2-aminopyrroles from enaminone–amidine adduct and phenacyl/benzyl/heteroalkyl-halides
المؤلفون: Hitesh B. Jalani, Arshi B. Baraiya, Dhaivat H. Pandya, Jayesh A. Sharma, Kamala K. Vasu, Jitendra C. Kaila, V. Sudarsanam, Amit N. Pandya
المصدر: Tetrahedron Letters. 52:6331-6335
بيانات النشر: Elsevier BV, 2011.
سنة النشر: 2011
مصطلحات موضوعية: Amidine, chemistry.chemical_compound, Chemistry, Intramolecular force, Organic Chemistry, Drug Discovery, Halide, Phenacyl, Biochemistry, Medicinal chemistry, Adduct
الوصف: Herein, we report an efficient and facile synthesis of substituted 2-aminopyrroles from the reaction of enaminone–amidine adduct and various phenacyl, benzyl, or heteroalkyl halides in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in good to excellent yields. The reaction proceeds through an intramolecular 5- exo trig cyclization resulting into diversely substituted 2-aminopyrroles.
تدمد: 0040-4039
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::744a91cce902daedfcd274935ad75cb5
https://doi.org/10.1016/j.tetlet.2011.08.149
حقوق: CLOSED
رقم الأكسشن: edsair.doi...........744a91cce902daedfcd274935ad75cb5
قاعدة البيانات: OpenAIRE