Meeting Organocatalysis with Drug Discovery: Asymmetric Synthesis of 3,3′-Spirooxindoles Fused with Tetrahydrothiopyrans as Novel p53-MDM2 Inhibitors-Reference-Cited by-同舟云学术

Meeting Organocatalysis with Drug Discovery: Asymmetric Synthesis of 3,3′-Spirooxindoles Fused with Tetrahydrothiopyrans as Novel p53-MDM2 Inhibitors

Published:2016-02-17 Issue:5 Volume:18 Page:1028-1031
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Shengzheng¹²,Jiang Yan¹,Wu Shanchao¹,Dong Guoqiang¹,Miao Zhenyuan¹,Zhang Wannian¹,Sheng Chunquan¹

Affiliation:

1. Department of Medicinal Chemistry, School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai 200433, People’s Republic of China

2. Department of Medicinal Chemistry, School of Pharmacy, Fourth Military Medical University, 169 Changle West Road, Xi’an, 710032, P.R. China

Funder

Ministry of Science and Technology of the People's Republic of China

Shanghai Municipal Education Commission

Shanghai Education Development Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b00155

Reference44 articles.

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

2. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

3. Horsfiline, an oxindole alkaloid from Horsfieldia superba

4. Biomimetic Total Synthesis of (+)-Gelsemine

5. Preparation and Synthetic Applications of 2-Halotryptamines: Synthesis of Elacomine and Isoelacomine

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