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One-Pot Reaction Sequence: N-Acylation/Pictet-Spengler Reaction/Intramolecular [4 + 2] Cycloaddition/Aromatization in the Synthesis of β-Carboline Alkaloid Analogues

Alekseeva K.A., Fedoseeva M.A., Bakhanovich O.V., Khrustalev V.N., Potkin V.I., Zhou H., Nikitina E.V., Zaytsev V.P., Zubkov F.I.

Дата публикации в реестре: 2025-05-27T14:17:13Z

Аннотация:
Ключевые слова:
Acylation, Alkaloids, Aromatic compounds, Cycloaddition, Maleic anhydride, aldimine, alkaloid derivative, beta carboline derivative, furan derivative, imine, maleic anhydride, pyrrole derivative, thiophene derivative, unclassified drug, Acylations, Azomethines, Isoindoles, One-pot reaction, One-pot synthesis, Pictet-Spengler reactions, Reaction sequences, Tryptamines, [4 + 2] cycloaddition, β-carboline, acylation, annulation reaction, aromatization, Article, cycloaddition, diastereoselectivity, Diels Alder reaction, isomerization, one pot synthesis, Pictet Spengler reaction, Cyclization

Тип: Article

Источник: Journal of Organic Chemistry

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