Journal
ORGANIC LETTERS
Volume 22, Issue 8, Pages 3195-3199Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c00969
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Funding
- National Key R&D Program of China [2017YFA0700103]
- NSFC [21672213, 21871258, 21922112]
- Strategic Priority Research Program of the Chinese Academy of Sciences [XDB20000000]
- Haixi Institute of CAS [CXZX-2017-P01]
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An iron-catalyzed radical alkylazidation of electron-deficient alkenes is reported. Alkyl diacyl peroxides work as the alkyl source, and trimethylsilyl azide acts as the azido reservoir. This method features mild reaction conditions, wide substrate scope, and good functional group tolerance, providing a range of alpha-azido esters, an alpha-azido ketone, and an alpha-azido cyanide in high yields. These azides can be easily transferred into many kinds of amino acid derivatives.
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