دورية أكاديمية

Electrocyclization and Unexpected Reactions of Non-Stabilized α,β:γ,δ-Unsaturated Azomethine Ylides: Experimental and Theoretical Studies.

التفاصيل البيبلوغرافية
العنوان: Electrocyclization and Unexpected Reactions of Non-Stabilized α,β:γ,δ-Unsaturated Azomethine Ylides: Experimental and Theoretical Studies.
المؤلفون: Molnár, István G.1 (AUTHOR), Mucsi, Zoltán2,3 (AUTHOR), Kovács, Ervin3,4 (AUTHOR), Nyerges, Miklós1 (AUTHOR)
المصدر: Synthesis. Sep2022, Vol. 54 Issue 17, p3845-3857. 13p.
مصطلحات موضوعية: *RING formation (Chemistry), *KINETIC control, *YLIDES, *CARBAZOLE derivatives, *CARBON-carbon bonds, *SCHIFF bases, *CARBAZOLE, *AZEPINES
مستخلص: Versatile, two-step syntheses of dihydrodibenzo[ c , e ]azepines, carbazole derivatives, and other alkaloid-type drug-like scaffolds by in situ generated azomethine ylide-induced intramolecular electrocyclization reaction from commercially available materials are presented. The reaction mechanisms of transition-metal-free carbon–carbon bond formation and the role of the kinetic control, resulting in the good regioselectivity, were confirmed by theoretical calculations. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:00397881
DOI:10.1055/a-1742-2005