scholarly journals The Fischer Indole Synthesis with Formic Acid.I.A Convenient Synthesis of 4a-Ethyl-9-formyl-1, 2, 3, 4, 4a, 9a-hexahydro-9H-carbazole

1967 ◽  
Vol 15 (4) ◽  
pp. 531-533 ◽  
Author(s):  
Yoshio Ban ◽  
Takeshi Oishi ◽  
Yoshiko Kishio ◽  
Ikuo Iijima
Molecules ◽  
2019 ◽  
Vol 24 (5) ◽  
pp. 960 ◽  
Author(s):  
Lei Peng ◽  
Xiaofei Zhang ◽  
Chunhao Yang

Bisindolyl alkaloids represent a large family of natural and synthetic products that display various biological activities. Among the bisindole compounds, 6,7,12,13-tetrahydro-5H-cyclohepta[2,1-b:3,4-b’]diindoles have received little attention. Only two methods have been developed for the construction of the 6,7,12,13-tetrahydro-5H-cyclohepta[2,1-b:3,4-b’]diindole scaffold thus far, including the classical Fischer indole synthesis conducted by reacting indole-fused cycloheptanone and hydrazines, and the condensation reaction to build the seven-membered ring. Here, we report for the first time a new route to synthesize 6,7,12,13-tetrahydro-5H-cyclohepta[2,1-b:3,4-b’]diindoles through intramolecular oxidative coupling of 1,3-di(1H-indol-3-yl)propanes in the presence of PIFA, DDQ and TMSCl with moderate to excellent yields.


2021 ◽  
Vol 23 (3) ◽  
pp. 1096-1102
Author(s):  
Hyunho Chung ◽  
Jeongyun Kim ◽  
Gisela A. González-Montiel ◽  
Paul Ha-Yeon Cheong ◽  
Hong Geun Lee

Author(s):  
Jianguo Xu ◽  
Jiangang Yu ◽  
Yi Jin ◽  
Jie Li ◽  
Zhiqun Yu ◽  
...  

1966 ◽  
Vol 14 (9) ◽  
pp. 934-939 ◽  
Author(s):  
Yuichi Kanaoka ◽  
Yoshio Ban ◽  
Koichi Miyashita ◽  
Kimiko Irie ◽  
Osamu Yonemitsu

2018 ◽  
Vol 61 (7-8) ◽  
pp. 685-688 ◽  
Author(s):  
Hien Vuong ◽  
Samantha Duarte ◽  
Douglas A. Klumpp

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