Enantioselective Nitroso Aldol Intramolecular Transesterification Cyclization Domino Reaction for Highly Effective Construction of Chiral Spirooxindoles-Reference-Cited by-同舟云学术

Enantioselective Nitroso Aldol Intramolecular Transesterification Cyclization Domino Reaction for Highly Effective Construction of Chiral Spirooxindoles

Published:2016-10-12 Issue:32 Volume:2016 Page:5437-5444
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Ji Shan-Ping¹²^ORCID,Liu Lin-Wei¹²,Chen Feng¹²,Ren Hong-Xia¹²,Yang Yu¹²,Zhang Zheng-Bing¹²,Peng Lin¹,Wang Li-Xin¹

Affiliation:

1. Key Laboratory of Asymmetric Synthesis and Chirotechnology of Sichuan Province; Chengdu Institute of Organic Chemistry; Chinese Academy of Sciences; 610041 Chengdu People's Republic of China

2. University of Chinese Academy of Sciences; 100039 Beijing P. R. China

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference45 articles.

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

2. Enantioselective Synthesis of AG-041R by using N-Heteroarenesulfonyl Cinchona Alkaloid Amides as Organocatalysts

3. Isolation, Structure Elucidation, and Biomimetic Total Synthesis of Versicolamide B, and the Isolation of Antipodal (−)-Stephacidin A and (+)-Notoamide B fromAspergillus versicolor NRRL 35600

4. Isolation, Structure Elucidation, and Biomimetic Total Synthesis of Versicolamide B, and the Isolation of Antipodal (−)-Stephacidin A and (+)-Notoamide B fromAspergillus versicolor NRRL 35600

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

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