A Gold-Catalyzed Domino Cyclization Enabling Rapid Construction of Diverse Polyheterocyclic Frameworks

We report herein an efficient gold(I)-catalyzed post-Ugi domino dearomatization/ipso-cyclization/Michael sequence that enables access to libraries of diverse (hetero)arene-annulated tricyclic heterocycles. This process affords novel complex polycyclic scaffolds in moderate to good yields from readily available acyclic precursors with excellent chemo-, regio-, and diastereoselectivity. The power of this strategy has been demonstrated by the rapid synthesis of 40 highly functionalized polyheterocycles bearing indole, pyrrole, (benzo)furan, (benzo)thiophene, pyrazole, and electron-rich arene groups in two operational steps. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Авторы
He Y.1 , Li Z.1 , Robeyns K.2 , Van Meervelt L. , Van Der Eycken E.V.
Номер выпуска
1
Язык
Английский
Страницы
272-276
Статус
Опубликовано
Том
57
Год
2018
Организации
  • 1 Laboratory for Organic and Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, KU Leuven, Celestijnenlaan 200F, Heverlee, Leuven, 3001, Belgium
  • 2 Institute of Condensed Matter and Nanosciences, MOST-Inorganic Chemistry, Université catholique de Louvain, Place L. Pasteur 1, Louvain-la-Neuve, 1348, Belgium
  • 3 Biomolecular Architecture, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, Heverlee, Leuven, 3001, Belgium
  • 4 Peoples Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya Street, Moscow, 117198, Russian Federation
Ключевые слова
dearomatization; domino cyclization; gold catalysis; heterocycles; Ugi reaction
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/6929/
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