Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 13, Issue 41, Pages 10295-10298Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ob01725d
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Funding
- National Natural Science Foundation of China [81421091]
- National Science Fund for Talent Training in Basic Science [J1103310]
- Qing Lan Project of Jiangsu Province
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A visible-light-promoted chloramination of olefins is reported. N-Chlorosulfonamides serve as both nitrogen and chlorine sources. These reactions provide a simple, efficient, regioselective, and atom-economical method for the preparation of vicinal haloamine derivatives under mild reaction conditions. A variety of olefins were tolerated, and chloramination products were obtained in good yields.
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