Palladium‐Catalyzed Tandem Carbonylative Aza‐Wacker‐Type Cyclization of Nucleophile Tethered Alkene to Access Fused N ‐Heterocycles-Reference-Cited by-同舟云学术

Palladium‐Catalyzed Tandem Carbonylative Aza‐Wacker‐Type Cyclization of Nucleophile Tethered Alkene to Access Fused N ‐Heterocycles

Published:2020-12-30 Issue:2 Volume:39 Page:317-322
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Shi Lijun¹²,Wen Mingshan¹,Li Fuwei¹

Affiliation:

1. State Key Laboratory for Oxo Synthesis and Selective Oxidation, Suzhou Research Institute of LICP, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences Lanzhou Gansu 730000 China

2. University of the Chinese Academy of Sciences Beijing 100049 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202000491

Reference43 articles.

1. Tandem Hydroaminomethylation Reaction to Synthesize Amines from Alkenes

2. Distal radical migration strategy: an emerging synthetic means

3. Achieving Molecular Complexity via Stereoselective Multiple Domino Reactions Promoted by a Secondary Amine Organocatalyst

4. Catalytic C–C Bond-Forming Multi-Component Cascade or Domino Reactions: Pushing the Boundaries of Complexity in Asymmetric Organocatalysis

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