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Design and Synthesis of New Biprivileged Molecular Scaffolds: Indolo-Fused Benzodiazepinyl/quinoxalinyl benzimidazoles

dc.citation.epage1684en_US
dc.citation.issue7en_US
dc.citation.volume7en_US
dc.citation.woscount4
dc.contributor.authorBarve, Indrajeet J.en_US
dc.contributor.authorChen, Chan-Yuen_US
dc.contributor.authorSalunke, Deepak B.en_US
dc.contributor.authorChung, Wen-Shengen_US
dc.contributor.authorSun, Chung-Mingen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:23:37Z
dc.date.available2014-12-08T15:23:37Z
dc.date.issued2012-06-01en_US
dc.description.abstractThe 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. PictetSpengler-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.en_US
dc.identifier.issn1861-4728en_US
dc.identifier.journalCHEMISTRY-AN ASIAN JOURNALen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/16516
dc.identifier.wosnumberWOS:000305239500032
dc.language.isoen_USen_US
dc.subjectdrug discoveryen_US
dc.subjectheterocyclesen_US
dc.subjectPictet-Spengler-type reactionsen_US
dc.subjectprivileged structuresen_US
dc.subjectsynthesis designen_US
dc.titleDesign and Synthesis of New Biprivileged Molecular Scaffolds: Indolo-Fused Benzodiazepinyl/quinoxalinyl benzimidazolesen_US
dc.typeArticleen_US

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