Journal
ORGANIC LETTERS
Volume 16, Issue 20, Pages 5458-5461Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol5027014
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Funding
- Natural Science Foundation of China [21390400, 21025208, 21202170, 21472193]
- National Basic Research Program of China [2012CB821600]
- National Program of Topnotch Young Professionals
- CAS Youth Innovation Promotion Association
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A new and efficient method for diazenylation reactions was developed with a Sc(OTf)(3)-catalyzed nitrogen-nitrogen bond cleavage process with triazenes. The transfer diazenylation reactions accommodate a diverse range of active methylene substrates including simple ketones to give aliphatic azo compounds that are of significant potential as azo prodrugs in high yields under mild conditions.
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