Show simple item record

Catalytic Ester and Amide to Amine Interconversion: Nickel-Catalyzed Decarbonylative Amination of Esters and Amides by C−O and C−C Bond Activation

dc.contributor.authorYue, Huifeng
dc.contributor.authorGuo, Lin
dc.contributor.authorLiao, Hsuan-Hung
dc.contributor.authorCai, Yunfei
dc.contributor.authorZhu, Chen
dc.contributor.authorRueping, Magnus
dc.date.accessioned2017-04-13T11:51:01Z
dc.date.available2017-04-13T11:51:01Z
dc.date.issued2017-03-15
dc.identifier.citationYue H, Guo L, Liao H-H, Cai Y, Zhu C, et al. (2017) Catalytic Ester and Amide to Amine Interconversion: Nickel-Catalyzed Decarbonylative Amination of Esters and Amides by C−O and C−C Bond Activation. Angewandte Chemie International Edition 56: 4282–4285. Available: http://dx.doi.org/10.1002/anie.201611819.
dc.identifier.issn1433-7851
dc.identifier.doi10.1002/anie.201611819
dc.identifier.doi10.1002/ange.201611819
dc.identifier.urihttp://hdl.handle.net/10754/623218
dc.description.abstractAn efficient nickel-catalyzed decarbonylative amination reaction of aryl and heteroaryl esters has been achieved for the first time. The new amination protocol allows the direct interconversion of esters and amides into the corresponding amines and represents a good alternative to classical rearrangements as well as cross coupling reactions.
dc.description.sponsorshipH.Y. and L.G. acknowledge the China Scholarship Council. H.-H.L. acknowledges the DAAD for a doctoral fellowship, Y.C. acknowledges the Alexander von Humboldt-Foundation for a fellowship. Support by King Abdullah University of Science and Technology (KAUST) is gratefully acknowledged.
dc.publisherWiley
dc.relation.urlhttp://onlinelibrary.wiley.com/doi/10.1002/anie.201611819/full
dc.rightsThis is the peer reviewed version of the following article: Catalytic Ester and Amide to Amine Interconversion: Nickel-Catalyzed Decarbonylative Amination of Esters and Amides by C-O and C-C Bond Activation, which has been published in final form at http://doi.org/10.1002/anie.201611819. This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving.
dc.subjectEsters
dc.subjectNickel
dc.subjectReaction Mechanisms
dc.subjectAmination
dc.subjectArenes
dc.titleCatalytic Ester and Amide to Amine Interconversion: Nickel-Catalyzed Decarbonylative Amination of Esters and Amides by C−O and C−C Bond Activation
dc.typeArticle
dc.contributor.departmentChemical Science Program
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.identifier.journalAngewandte Chemie
dc.eprint.versionPost-print
dc.contributor.institutionInstitute of Organic Chemistry; RWTH Aachen University; Landoltweg 1 52074 Aachen Germany
kaust.personRueping, Magnus
refterms.dateFOA2018-03-15T00:00:00Z
dc.date.published-online2017-03-15
dc.date.published-print2017-04-03


Files in this item

Thumbnail
Name:
Manuscript_Accepted.pdf
Size:
457.7Kb
Format:
PDF
Description:
Accepted Manuscript
Download

This item appears in the following Collection(s)

Show simple item record