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Verfasst von:Antoni, Patrick W. [VerfasserIn]   i
 Mackenroth, Alexandra [VerfasserIn]   i
 Mulks, Florian [VerfasserIn]   i
 Rudolph, Matthias [VerfasserIn]   i
 Helmchen, Günter [VerfasserIn]   i
 Hashmi, A. Stephen K. [VerfasserIn]   i
Titel:Dibenzothiophenesulfilimines
Titelzusatz:a convenient approach to intermolecular rhodium-catalysed C−H amidation
Verf.angabe:Patrick W. Antoni, Alexandra V. Mackenroth, Florian F. Mulks, Matthias Rudolph, Günter Helmchen, and A. Stephen K. Hashmi
E-Jahr:2020
Jahr:June 9, 2020
Umfang:4 S.
Fussnoten:Gesehen am 02.09.2020
Titel Quelle:Enthalten in: Chemistry - a European journal
Ort Quelle:Weinheim : Wiley-VCH, 1995
Jahr Quelle:2020
Band/Heft Quelle:26(2020), 37, Seite 8235-8238
ISSN Quelle:1521-3765
Abstract:A sulfilimine‐based Group 9 transition‐metal‐catalysed C−H amidation procedure is reported. Dibenzothiophene‐based sulfilimines were shown to constitute a class of novel amidation reagents which enable the transfer of a wide range of N‐sulfonyl and N‐acyl moieties. It was demonstrated that sulfilimines, which are easily accessible from cheap reagents, are safe‐to‐handle and represent broadly applicable amidation reagents. The dibenzothiophene can be recycled after use. The C−H amidation was shown to proceed with high selectivity and gave the mono‐amidated products, mostly in good to excellent yields.
DOI:doi:10.1002/chem.202002371
URL:kostenfrei: Volltext ; Verlag: https://doi.org/10.1002/chem.202002371
 kostenfrei: Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/chem.202002371
 DOI: https://doi.org/10.1002/chem.202002371
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:amidation
 C−H activation
 homogeneous catalysis
 rhodium
 sulfilimines
 transition-metal catalysis
K10plus-PPN:1728603838
Verknüpfungen:→ Zeitschrift
 
 
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