Amidinyl radicals: new and useful intermediates for the synthesis of imidazolines and imidazoles
Literature Information
Publication Date
2003-06-23
DOI
10.1039/B304545E
Impact Factor
6.222
Authors
Dominique Gennet, Samir Z. Zard, Haiwen Zhang
View Original
Abstract
Amidinyl radicals are readily generated from amidoxime benzoates by treatment with a stannane–diazo initiator or with Ni–AcOH and captured by an internal olefin to give the corresponding imidazoline.
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Source Journal
Chemical Communications
CiteScore:
8.6
Self-citation Rate:
4.7%
Articles per Year:
2458
ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry
Recommended Compounds
![N-[(1-Ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-5-sulfamoylbenzamide structure](https://static.chemtradehub.com/structs/673/67381-52-6-877f.webp "N-[(1-Ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-5-sulfamoylbenzamide structure")
N-[(1-Ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-5-sulfamoylbenzamide
CAS Number:
67381-52-6
Molecular Formula:
C14H21N3O4S
5-(6-Methoxy-1-benzofuran-2-yl)-2-(3-methyl-2-buten-1-yl)-1,3-benzenediol
CAS Number:
1017277-40-5
Molecular Formula:
C20H20O4
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