Pd‐Catalyzed 2, 3‐Allenylation of Oxindoles with 2, 3‐Allenylic Carbonates-Reference-Cited by-同舟云学术

Pd‐Catalyzed 2, 3‐Allenylation of Oxindoles with 2, 3‐Allenylic Carbonates

Published:2021-08-24 Issue:11 Volume:39 Page:3044-3050
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Lin Jie¹,Jia Minqiang¹,Ma Shengming¹²

Affiliation:

1. Research Center for Molecular Recognition and Synthesis, Department of Chemistry Fudan University 220 Handan Lu Shanghai 200433 China

2. State Key Laboratory of Organometallic Chemistry Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu Shanghai 200032 China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202100402

Reference122 articles.

1. For selected reviews on natural products and bioactive compounds containing oxindole scaffolds see: (a) Marti C.; Carreira E. M. Construction of Spiro[pyrrolidine‐3 3’‐oxindoles]‐Recent Applications to the Synthesis of Oxindole Alkaloids.Eur. J. Org. Chem.2003 2209–2219;

2. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

3. 3-Substituted-3-hydroxy-2-oxindole, an Emerging New Scaffold for Drug Discovery with Potential Anti-Cancer and other Biological Activities

4. 3‐Alkenyl‐oxindoles: Natural Products, Pharmaceuticals, and Recent Synthetic Advances in Tandem/Telescoped Approaches

5. Horsfiline, an oxindole alkaloid from Horsfieldia superba

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