Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/97105
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dc.contributor.authorZhang, Feng-Lianen
dc.contributor.authorWang, Yi-Fengen
dc.contributor.authorLonca, Geoffroy Hervéen
dc.contributor.authorZhu, Xuen
dc.contributor.authorChiba, Shunsukeen
dc.date.accessioned2014-06-11T03:09:39Zen
dc.date.accessioned2019-12-06T19:38:59Z-
dc.date.available2014-06-11T03:09:39Zen
dc.date.available2019-12-06T19:38:59Z-
dc.date.copyright2014en
dc.date.issued2014en
dc.identifier.citationZhang, F.-L., Wang, Y.-F., Lonca, G. H., Zhu, X., & Chiba, S. (2014). Amide Synthesis by Nucleophilic Attack of Vinyl Azides. Angewandte Chemie International Edition, 53(17), 4390-4394.en
dc.identifier.issn1433-7851en
dc.identifier.urihttps://hdl.handle.net/10356/97105-
dc.description.abstractA method for the synthesis of amide-containing molecules was developed using vinyl azides as an enamine-type nucleophile towards carbon electrophiles, such as imines, aldehydes, and carbocations that were generated from alcohols in the presence of BF3⋅OEt2. After nucleophilic attack of the vinyl azide, a substituent of the resulting iminodiazonium ion intermediate migrates to form a nitrilium ion, which is hydrolyzed to afford the corresponding amide.en
dc.language.isoenen
dc.relation.ispartofseriesAngewandte chemie international editionen
dc.rights© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en
dc.subjectDRNTU::Science::Chemistry::Inorganic chemistry::Synthesisen
dc.titleAmide synthesis by nucleophilic attack of vinyl azidesen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1002/anie.201400938en
item.grantfulltextnone-
item.fulltextNo Fulltext-
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