Investigation on the Se-Acylation with N-Acylbenzotriazoles |
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Authors: | Junyan Jiang Wencun Wang Xiaoxia Wang Xiangming Zhu Zhifang Li |
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Institution: | 1. College of Chemistry and Life Sciences , Zhejiang Normal University , Jinhua, P.R. China;2. Key Laboratory of Organosilicon Chemistry and Material Technology , Ministry of Educations, Hangzhou Normal University , Hangzhou, P.R. China |
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Abstract: | Abstract The acylation of Se-nucleophiles with N-acylbenzotriazoles was investigated. Samarium phenylselenolate and benzylselenolate (RSeSmI2) reacted with N-aroyl and N-alkanoylbenzotriazoles smoothly and afforded the corresponding selenol esters in good yields. Treatment of the RSeSmI2 with α,β-unsaturated N-acylbenzotriazoles afforded the anticipated α,β-unsaturated selenol esters in moderate yields, due mainly to the side reaction of conjugate addition. GRAPHICAL ABSTRACT ![id=](/na101/home/literatum/publisher/tandf/journals/content/gpss20/2011/gpss20.v186.i10/10426507.2010.540605/production/images/medium/gpss_a_540605_o_uf0001.gif) |
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Keywords: | N-Acylbenzotriazole samarium(II) iodide diselenides Se-acylation selenol esters |
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