Design and synthesis of new biprivileged molecular scaffolds: Indolo-fused benzodiazepinyl/quinoxalinyl benzimidazoles

Indrajeet J. Barve, Chan Yu Chen, Deepak B. Salunke, Wen-Sheng Chung*, Chung-Ming Sun

*此作品的通信作者

研究成果: Article同行評審

19 引文 斯高帕斯(Scopus)

摘要

The present article describes the design and synthesis of new biprivileged molecular scaffolds with diverse structural features. Commercially available, simple heterocyclic building blocks such as 4-fluoro-3-nitrobenzoic acid, 2-chloro-3-nitrobenzoic acid, and indoline were utilized for the synthesis of the novel heterocycles. Pictet-Spengler-type condensation was used as a key step to construct tetracyclic indolo-benzodiazepines and indolo-quinoxalines linked with substituted benzimidazoles. Analysis of single crystals of representative compounds showed that these molecular skeletons have the potential to present various substituents with distinct three-dimensional orientations.

原文English
頁(從 - 到)1684-1690
頁數7
期刊Chemistry - An Asian Journal
7
發行號7
DOIs
出版狀態Published - 1 6月 2012

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