Diastereo- and Enantioselective Construction of 3,3′-Pyrrolidinyldispirooxindole Framework via Catalytic Asymmetric 1,3-Dipolar Cycloadditions-Reference-Cited by-同舟云学术

Diastereo- and Enantioselective Construction of 3,3′-Pyrrolidinyldispirooxindole Framework via Catalytic Asymmetric 1,3-Dipolar Cycloadditions

Published:2015-05-14 Issue:11 Volume:80 Page:5737-5744
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dai Wei¹,Jiang Xiao-Li¹,Wu Qiong²,Shi Feng¹,Tu Shu-Jiang¹

Affiliation:

1. Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, School of Chemistry & Chemical Engineering, Jiangsu Normal University, Xuzhou 221116, China

2. School of Chemistry and Chemical Engineering, Xuzhou Institute of Technology, Xuzhou 221008, China

Funder

National Natural Science Foundation of China

Jiangsu Province

Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, Jiangsu Normal University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b00708

Reference66 articles.

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

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

3. Horsfiline, an oxindole alkaloid from Horsfieldia superba

4. Novel mammalian cell cycle inhibitors, spirotryprostatins A and B, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase

5. Structure-guided identification of novel VEGFR-2 kinase inhibitors via solution phase parallel synthesis

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