Controllable Synthesis of Polyheterocyclic Spirooxindoles and 3,3‐Bistryptophol Oxindoles via Fe(ClO 4 ) 3 ⋅ 6H 2 O‐Promoted Hetero‐Pictet‐Spengler Reaction-Reference-Cited by-同舟云学术

Controllable Synthesis of Polyheterocyclic Spirooxindoles and 3,3‐Bistryptophol Oxindoles via Fe(ClO 4 ) 3 ⋅ 6H 2 O‐Promoted Hetero‐Pictet‐Spengler Reaction

Published:2019-12-04 Issue:3 Volume:362 Page:500-505
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Song Jun‐Rong¹²,Li Zhi‐Yao³,Wang Guang‐Di³,Zhang Ni¹²,Chen Chao¹²,Chen Juan¹²,Ren Hai¹²,Pan Weidong¹²³

Affiliation:

1. State key Laboratory of Functions and Applications of Medicinal Plants Guizhou Medical University Guiyang 550014 People's Republic of China

2. The Key Laboratory of Chemistry for Natural Products of Guizhou Province and Chinese Academy of Sciences / Guizhou Provincial Engineering Research Center for Natural Drugs Guiyang 550014 People's Republic of China

3. Guizhou University Huaxi Avenue South Guiyang 550025 People's Republic of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201901346

Reference68 articles.

2. 3-Substituted-3-hydroxy-2-oxindole, an Emerging New Scaffold for Drug Discovery with Potential Anti-Cancer and other Biological Activities

3. Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products

4. Synthesis and Antitumor Effect in Vitro and in Vivo of Substituted 1,3-Dihydroindole-2-ones

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