Journal
CHEMISTRY-AN ASIAN JOURNAL
Volume 12, Issue 6, Pages 713-717Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.201700017
Keywords
alkenes; amidoselenation; amidotelluration; difunctionalization; oxygen
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Funding
- National Natural Science Foundation of China [U1504210]
- Program for Innovative Research Team of Science and Technology in the University of Henan Province [16IRTSTHN003]
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A protocol has been established for oxygen-mediated amidoselenation and amidotelluration of alkenes under mild conditions. This method provides a simple route to a series of structurally diverse beta-amido selenides and beta-amido tellurides in moderate to high yields. The wide substrate scope, good functional group tolerance, ease of large-scale preparation and potential for product derivatization make this reaction attractive for the synthesis of nitrogen-, selenium- and tellurium-containing molecules.
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