Catalytic Thia-Sommelet−Hauser Rearrangement: Application to the Synthesis of Oxindoles-Reference-Cited by-同舟云学术

Catalytic Thia-Sommelet−Hauser Rearrangement: Application to the Synthesis of Oxindoles

Published:2011-02-09 Issue:5 Volume:13 Page:1210-1213
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Yuye¹,Shi Yi¹,Huang Zhongxing¹,Wu Xinhu¹,Xu Pengfei¹,Wang Jianbo¹,Zhang Yan¹

Affiliation:

1. Beijing National Laboratory of Molecular Sciences (BNLMS) and Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China, and State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol200091k

Reference80 articles.

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

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

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

4. Indol-2-one Intermediates: Mechanistic Evidence and Synthetic Utility. Total Syntheses of (±)-Flustramines A and C

5. Synthesis of the Bicyclic Welwitindolinone Core via an Alkylation/Cyclization Cascade Reaction

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