Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-33034
Atanassov, P K; Linden, A; Heimgartner, H (2010). Synthesis of 1,3-Selenazol-2(3H)-imines. Helvetica Chimica Acta, 93(3):395-404.
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The reaction of N,N’-diarylselenoureas 16 with phenacyl bromide in EtOH under reflux, followed by treatment with NH3 , gave N,3-diaryl-4-phenyl-1,3-selenazol-2(3H)-imines 13 in high yields (Scheme 2). A reaction mechanism via formation of the corresponding Se-(benzoylmethyl)isoselenoureas 18 and
subsequent cyclocondensation is proposed (Scheme 3). The N,N’-diarylselenoureas 16 were conveniently prepared by the reaction of aryl isoselenocyanates 15 with 4-substituted anilines. The structures of 13a and 13c were established by X-ray crystallography.
|Item Type:||Journal Article, refereed, original work|
|Communities & Collections:||07 Faculty of Science > Department of Chemistry|
|Date:||11 March 2010|
|Deposited On:||26 Mar 2010 14:08|
|Last Modified:||05 Jun 2014 13:06|
|Publisher:||Verlag Helvetica Chimica Acta|
Scopus®. Citation Count: 5
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