Radical cyclizations involving the evolution of nitrogen

被引:18
作者
Kim, S
机构
[1] Department of Chemistry, Korea Adv. Inst. Sci. and Technol.
关键词
D O I
10.1351/pac199668030623
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The radical cyclizations of N-aziridinyl imines and alkyl azides provided reliable methods for the formation of five- and six-membered carbon-centered and nitrogen-centered radicals from acyclic precursors. N-Aziridinyl imino and azido groups were utilized as radical precursors as well as radical accepters in radical cyclization. Furthermore, intramolecular addition of aminyl radicals to carbonyl groups proceeded cleanly, yielding 1,5-acyl group transfer from carbon to nitrogen.
引用
收藏
页码:623 / 626
页数:4
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