دورية أكاديمية

Synthesis of dibenzosuberenone-based novel polycyclic π-conjugated dihydropyridazines, pyridazines and pyrroles

التفاصيل البيبلوغرافية
العنوان: Synthesis of dibenzosuberenone-based novel polycyclic π-conjugated dihydropyridazines, pyridazines and pyrroles
المؤلفون: Ramazan Koçak, Arif Daştan
المصدر: Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 719-729 (2021)
بيانات النشر: Beilstein-Institut, 2021.
سنة النشر: 2021
المجموعة: LCC:Science
LCC:Organic chemistry
مصطلحات موضوعية: dibenzosuberenone, inverse electron-demand diels–alder cycloaddition reactions, p-quinone methide, polycyclic π-conjugated dihydropyridazines, pyridazines, pyrroles, Science, Organic chemistry, QD241-441
الوصف: The synthesis of novel polycyclic π-conjugated dihydropyridazines, pyridazines, and pyrroles was studied. Dihydropyridazine dyes were synthesized by inverse electron-demand Diels–Alder cycloaddition reactions between a dibenzosuberenone and tetrazines that bear various substituents. The pyridazines were synthesized in high yields by oxidation of dihydropyridazine-appended dibenzosuberenones with PIFA or NO. p-Quinone derivatives of pyridazines were also obtained by H-shift isomerization following the inverse electron-demand Diels–Alder reaction of tetrazines with p-quinone dibenzosuberenone. Then these pyridazines were converted to the corresponding pyrroles by reductive treatment with zinc. It was observed that all the dihydropyridazines obtained gave absorbance and emission at long wavelengths.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1860-5397
Relation: https://doaj.org/toc/1860-5397
DOI: 10.3762/bjoc.17.61
URL الوصول: https://doaj.org/article/43a6f6202c8e43cfa9dfc37bcaf75491
رقم الأكسشن: edsdoj.43a6f6202c8e43cfa9dfc37bcaf75491
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:18605397
DOI:10.3762/bjoc.17.61