دورية أكاديمية
Synthesis of dibenzosuberenone-based novel polycyclic π-conjugated dihydropyridazines, pyridazines and pyrroles
العنوان: | Synthesis of dibenzosuberenone-based novel polycyclic π-conjugated dihydropyridazines, pyridazines and pyrroles |
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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 |
تدمد: | 18605397 |
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DOI: | 10.3762/bjoc.17.61 |