Facile Synthesis of Azaarene-Substituted 3-Hydroxy-2-oxindoles via Brønsted Acid Catalyzed sp3 C–H Functionalization-Reference-Cited by-同舟云学术

Facile Synthesis of Azaarene-Substituted 3-Hydroxy-2-oxindoles via Brønsted Acid Catalyzed sp3 C–H Functionalization

Published:2012-01-24 Issue:3 Volume:14 Page:676-679
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Niu Rui¹,Xiao Jian¹,Liang Tao¹,Li Xingwei¹

Affiliation:

1. Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, P. R. China, and Key Laboratory of Marine Environment and Ecology, Ministry of Education, and College of Environmental Science and Engineering, Ocean University of China, Qingdao 266100, P. R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol2030982

Reference65 articles.

1. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

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

3. Gelsemine: A Thought-Provoking Target for Total Synthesis

4. The Asymmetric Intramolecular Heck Reaction in Natural Product Total Synthesis

5. 3-Substituted-3-hydroxy-2-oxindole, an Emerging New Scaffold for Drug Discovery with Potential Anti-Cancer and other Biological Activities

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