Expedient Approach for the Synthesis of Trispiropyrrolidine Bisoxindoles Through 1,3-Dipolar Cycloaddition Reactions-Reference-Cited by-同舟云学术

Expedient Approach for the Synthesis of Trispiropyrrolidine Bisoxindoles Through 1,3-Dipolar Cycloaddition Reactions

Published:2015-03-19 Issue:10 Volume:45 Page:1259-1268
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Feng Guo-Liang¹,Li Yue¹,Geng Li-Jun¹,Zhang Hong-Li¹,Shi Yan-Jing¹,Wang Kai-Fang²

Affiliation:

1. School of Science, Hebei University of Science and Technology, Shijiazhuang, China

2. Shijiazhuang Yonggangfangjong Co., Electronic Materials, Shijiazhuang, China

Funder

We gratefully acknowledge financial support from the Natural Science Foundation of Hebei Province No. (B2012208051), and the Research Foundation of Hebei University of Science and Technology. No. (YY15).

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2015.1014915

Reference20 articles.

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2. Grigg, R.; Sridharan, V. In Advances in Cycloaddition; Curran, D. P. (Ed.); Jai Press: London, 1993; vol. 3, pp. 161–204.

3. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3+2]-Cycloaddition of Azomethine Ylides

4. The Three-Component Reaction between Isatin,α-Amino Acids, and Dipolarophiles

5. Asymmetric, stereocontrolled total synthesis of (+) and (−)-spirotryprostatin B via a diastereoselective azomethine ylide [1,3]-dipolar cycloaddition reaction

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