Weak-coordination-auxiliary aminocatalysis enables directed [3 + 2] cyclization for 2-acylindolizines-Reference-Cited by-同舟云学术

Weak-coordination-auxiliary aminocatalysis enables directed [3 + 2] cyclization for 2-acylindolizines

Published:2024 Issue: Volume: Page:
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Zeng Kui¹^ORCID,Pandit Neeraj Kumar²^ORCID,Oliveira João C. A.²,Dechert Sebastian³^ORCID,Ackermann Lutz²⁴⁵^ORCID,Zhang Kai¹^ORCID

Affiliation:

1. Sustainable Materials and Chemistry, Dept. Wood Technology and Wood-Based Composites, University of Göttingen, Göttingen, Germany

2. Institute of Organic and Biomolecular Chemistry, University of Göttingen, Göttingen, Germany

3. Institute of Inorganic Chemistry, University of Göttingen, Göttingen, Germany

4. Wöhler Research Institute for Sustainable Chemistry (WISCh), University of Göttingen, Göttingen, Germany

5. DZHK (German Centre for Cardiovascular Research), Potsdamer Straße 58, 10785 Berlin, Germany

Abstract

A weak-coordination-auxiliary amino-catalyzed approach enables directed [3 + 2] cyclization of α,β-unsaturated ketones and N-heteroaryl ketones for the desired 2-acylindolizines via an iminium ion/enamine tandem sequence.

Funder

Georg-August-Universität Göttingen

China Scholarship Council

H2020 European Research Council

Deutsche Forschungsgemeinschaft

Deutsches Zentrum für Herz-Kreislaufforschung

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/GC/D3GC03552B

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