期刊
ORGANIC LETTERS
卷 15, 期 17, 页码 4616-4619出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol4023112
关键词
-
资金
- EPSRC [EP/J007455/1, EP/G036764/1]
- Bristol Chemical Synthesis CDT
- Royal Society for a University Research Fellowship
- EPSRC [EP/K03927X/1, EP/J007455/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [981192, EP/J007455/1, EP/K03927X/1] Funding Source: researchfish
Pd-catalyzed cyclizations of oxime esters with 1,2-dialkylated alkenes provide an entry to chiral dihydropyrroles. Substrate and catalyst controlled strategies for selective product formation (vs alternative pyrroles) are outlined.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据
分享论文
