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One-Pot Synthesis of Highly Substituted Polyheteroaromatic Compounds by Rhodium(III)-Catalyzed Multiple C-H Activation and Annulation

dc.citation.epage9892en_US
dc.citation.issue37en_US
dc.citation.spage9889en_US
dc.citation.volume53en_US
dc.citation.woscount6
dc.contributor.authorJayakumar, Jayachandranen_US
dc.contributor.authorParthasarathy, Kanniyappanen_US
dc.contributor.authorChen, Yi-Hsiangen_US
dc.contributor.authorLee, Tai-Huaen_US
dc.contributor.authorChuang, Shih-Chingen_US
dc.contributor.authorCheng, Chien-Hongen_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:36:48Z
dc.date.available2014-12-08T15:36:48Z
dc.date.issued2014-09-08en_US
dc.description.abstractA new method for the synthesis of highly substituted naphthyridine-based polyheteroaromatic compounds in high yields proceeds through rhodium(III)-catalyzed multiple CH bond cleavage and CC and CN bond formation in a one-pot process. Such highly substituted polyheteroaromatic compounds have attracted much attention because of their unique -conjugation, which make them suitable materials for organic semiconductors and luminescent materials. Furthermore, a possible mechanism, which involves multiple chelation-assisted ortho CH activation, alkyne insertion, and reductive elimination, is proposed for this transformation.en_US
dc.identifier.doi10.1002/anie.201405183en_US
dc.identifier.issn1433-7851en_US
dc.identifier.journalANGEWANDTE CHEMIE-INTERNATIONAL EDITIONen_US
dc.identifier.urihttp://dx.doi.org/10.1002/anie.201405183en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/25180
dc.identifier.wosnumberWOS:000342678200036
dc.language.isoen_USen_US
dc.subjectalkynesen_US
dc.subjectannulationen_US
dc.subjectbenzamidinesen_US
dc.subjectCH activationen_US
dc.subjectrhodiumen_US
dc.titleOne-Pot Synthesis of Highly Substituted Polyheteroaromatic Compounds by Rhodium(III)-Catalyzed Multiple C-H Activation and Annulationen_US
dc.typeArticleen_US

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