期刊
ORGANIC LETTERS
卷 16, 期 6, 页码 1814-1817出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol500567t
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资金
- DST, New Delhi
- JCB Fellowship [SR/S2/JCB-11/2008]
A novel strategy for the direct conversion of aryl- and heteroarylamines to selenides has been developed via diazotization of amines with tert-butyl nitrite in neutral medium followed by reaction with diaryl/diheteroaryl/dialkyl diselenides in one pot under photocatalysis at room temperature in the absence of any metal. This reaction is also applied for the synthesis of tellurides. The selenylation of heteroarylamine by this protocol is of much significance because of the difficulty in diazotization of these molecules by a standard diazotization method in acid medium.
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