Synthesis of indolizidines from dialkylated isocyanides: a novel radical cyclisation/N-alkylation/ring closing metathesis approach

被引:18
作者
Lamberto, Massimiliano [1 ,2 ]
Kilburn, Jeremy D. [1 ]
机构
[1] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
[2] Monmouth Univ, Dept Chem Med Technol & Phys, W Long Branch, NJ 07764 USA
关键词
D O I
10.1016/j.tetlet.2008.08.088
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Two dialkylated isocyanides were first synthesised from simple starting materials and then used as building blocks for the synthesis of indolizidines via a novel radical cyclisation/N-alkylation/ring closing metathesis strategy. Several functionalised indolizidines were accessed in good to excellent yields. (c) 2008 Elsevier Ltd. All Fights reserved.
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页码:6364 / 6367
页数:4
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