A Pd‐Catalyzed Annulation Strategy to Linearly Fused Functionalized N‐Heterocycles

Abstract: Linearly fused polycyclic piperidines represent common substructures in natural products and biologically active small molecules. We have devised a Pd‐catalyzed annulation strategy to these compounds that converts readily available 2‐tetralones and indanones into these scaffolds with the potential for control of both enantio‐ and diastereoselectivity. Importantly, these compounds can be chemoselectively functionalized, providing an efficient and robust methodology to these important nitrogen‐containing molecules.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
A Pd‐Catalyzed Annulation Strategy to Linearly Fused Functionalized N‐Heterocycles ; day:20 ; month:02 ; year:2024 ; extent:7
Chemistry - a European journal ; (20.02.2024) (gesamt 7)

Creator
Hoteite, Larry
Allen, Benjamin D. W.
Elhajj, Ms. Ergaiya A.
Meijer, Anthony J. H. M.
Harrity, Joseph P. A.

DOI
10.1002/chem.202400116
URN
urn:nbn:de:101:1-2024022114591797827266
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 11:01 AM CEST

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Associated

  • Hoteite, Larry
  • Allen, Benjamin D. W.
  • Elhajj, Ms. Ergaiya A.
  • Meijer, Anthony J. H. M.
  • Harrity, Joseph P. A.

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