期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 132, 期 49, 页码 17511-17515出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja1068036
关键词
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资金
- Swiss National Science Foundation [21-67106.01, 7SUPJ062348]
The radical-mediated carboazidation of terminal alkenes using electrophilic alkanesulfonyl azides is reported. A single reagent delivers the necessary electrophilic alkyl radical as well as the azido group, and good yields are obtained by using a moderate excess of the carboazidating reagent (1.5-2 equiv). Interestingly, in addition to the starting sulfonyl azide, this method requires only the use of a radical initiator, di-tert-butyldiazene. In terms of atom economy, this azide transfer reaction is close to ideal, as SO2 (1 equiv) is the only side product. The synthetic potential of this process has been demonstrated by a formal synthesis of the alkaloid lepadiformine C.
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