4.4 Article

Catalyst-controlled exo/endo selectivity in a post-Ugi intramolecular hydroarylation: synthesis of pyrrolopyridinones, pyrroloazepinones, and benzothienopyridines

期刊

TETRAHEDRON
卷 71, 期 21, 页码 3333-3342

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2015.03.103

关键词

Synthetic methods; Multicomponent reactions; Regioselective; Heterocycles; Hydroarylation

资金

  1. F.W.O [Fund for Scientific Research Flanders (Belgium)]
  2. Research Fund of the University of Leuven (KU Leuven)
  3. CSC (China Scholarship Council)
  4. EMA2experts (Erasmus Mundus Action 2, Lot 11 Asia: Experts)

向作者/读者索取更多资源

A facile catalyst-controlled regioselective post-Ugi intramolecular hydroarylation lished, which delivers an expedient access to biologically significant heterocycles idinones, pyrroloazepinones, and benzothienopyridines. (C) 2015 Elsevier Ltd. All rights reserved.

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