Efficient 1,6-addition reactions of 3-substituted oxindoles: Access to isoxazole-fused 3,3′-disubstituted oxindole scaffolds and hexahydro-1h-pyrido[2,3-b]indol-2-one scaffolds-Reference-Cited by-同舟云学术

Efficient 1,6-addition reactions of 3-substituted oxindoles: Access to isoxazole-fused 3,3′-disubstituted oxindole scaffolds and hexahydro-1h-pyrido[2,3-b]indol-2-one scaffolds

Published:2018-05-23 Issue:12 Volume:48 Page:1454-1464
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Liu Xiong-Wei¹,Yao Zhen¹,Wang Guan-Lian¹,Chen Zhi-Yong¹,Liu Xiong-Li¹²,Tian Min-Yi¹,Wei Qi-Di¹,Zhou Ying²,Zhang Jian-Fei¹

Affiliation:

1. Guizhou Engineering Center for Innovative Traditional Chinese Medicine and Ethnic Medicine, Guizhou University, Guiyang, China

2. School of Pharmacy, Guiyang College of Traditional Chinese Medicine, Guiyang, China

Funder

National Natural Science Foundation of China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2018.1454475

Reference16 articles.

1. Neoxaline, a new alkaloid produced by Aspergillus japonicus. Production, isolation and properties.

2. The isolation, structure and absolute configuration of secalonic acid D, the toxic metabolite of Penicillium oxalicum

3. Kapakahine B, a cyclic hexapeptide with an .alpha.-carboline ring system from the marine sponge Cribrochalina olemda

4. Conjugate addition reactions of carbon nucleophiles to electron-deficient dienes

5. An Improved Synthesis of 3-Methyl-4-nitro-5-heteroarylethenylisoxazoles

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