Organocatalytic oxa/aza-Michael–Michael Cascade Strategy for the Construction of Spiro [Chroman/Tetrahydroquinoline-3,3′-oxindole] Scaffolds-Reference-Cited by-同舟云学术

Organocatalytic oxa/aza-Michael–Michael Cascade Strategy for the Construction of Spiro [Chroman/Tetrahydroquinoline-3,3′-oxindole] Scaffolds

Published:2013-07-30 Issue:16 Volume:15 Page:4062-4065
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Mao Haibin¹,Lin Aijun¹,Tang Yang¹,Shi Yan¹,Hu Hongwen¹,Cheng Yixiang¹,Zhu Chengjian¹

Affiliation:

1. School of Chemistry and Chemical Engineering, State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing, 210093, China, and Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, 200032, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol401595g

Reference48 articles.

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

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

3. Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position

4. Strategies for the enantioselective synthesis of spirooxindoles

5. Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks

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