Isatin N,N′-Cyclic Azomethine Imine 1,3-Dipole and Base Catalyzed Michael Addition with β-Nitrostyrene via C3 Umpolung of Oxindole-Reference-Cited by-同舟云学术

Isatin N,N′-Cyclic Azomethine Imine 1,3-Dipole and Base Catalyzed Michael Addition with β-Nitrostyrene via C3 Umpolung of Oxindole

Published:2017-06-01 Issue:12 Volume:19 Page:3051-3054
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Xiao¹²,Wu Lin¹²,Yang Peng¹²,Song Xiang-Jia¹²,Ren Hong-Xia¹²,Peng Lin¹,Wang Li-Xin¹^ORCID

Affiliation:

1. Key Laboratory of Asymmetric Synthesis and Chirotechnology of Sichuan Province, Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu 610041, China

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

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b01063

Reference57 articles.

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

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

3. Transition‐Metal‐Mediated Routes to 3,3‐Disubstituted Oxindoles through Anilide Cyclisation

4. Recent advances in organocatalytic methods for the synthesis of disubstituted 2- and 3-indolinones

5. Recent progress in enantioselective synthesis of C3-functionalized oxindoles: rare earth metals take action

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