Convenient synthesis of polysubstituted 3-iodofurans through the tandem ring-opening/cyclization reaction of 1-alkynyl-2,3-epoxy alcohols
文献类型:期刊论文
作者 | Liu WM(刘维民)![]() |
刊名 | SYNTHESIS-STUTTGART
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出版日期 | 2007 |
期号 | 21页码:3295-3300 |
关键词 | iodofuran tandem reaction epoxide electrophilic cyclization |
ISSN号 | 0039-7881 |
通讯作者 | 梁永民 |
中文摘要 | A novel method for the synthesis of highly substituted iodine-containing furans has been developed by the cyclization of 1-(aryl ethynyl)-2,3 -epoxy alcohols (1-aryl-4,5-epoxyalk-1-yn-3-ols) with alcohols as nucleophiles under very mild reaction conditions. The resulting iodine-containing furans can be readily elaborated to more complex products using known organopalladium chemistry. |
学科主题 | 材料科学与物理化学 |
收录类别 | SCI |
资助信息 | the NSFC (NSFC-20621091;NSFC-20672049);the “Hundred Scientist Program” from the Chinese Academy of Sciences |
语种 | 英语 |
WOS记录号 | WOS:000251087900004 |
公开日期 | 2013-11-01 |
源URL | [http://210.77.64.217/handle/362003/4015] ![]() |
专题 | 兰州化学物理研究所_固体润滑国家重点实验室 |
推荐引用方式 GB/T 7714 | Liu WM. Convenient synthesis of polysubstituted 3-iodofurans through the tandem ring-opening/cyclization reaction of 1-alkynyl-2,3-epoxy alcohols[J]. SYNTHESIS-STUTTGART,2007(21):3295-3300. |
APA | 刘维民.(2007).Convenient synthesis of polysubstituted 3-iodofurans through the tandem ring-opening/cyclization reaction of 1-alkynyl-2,3-epoxy alcohols.SYNTHESIS-STUTTGART(21),3295-3300. |
MLA | 刘维民."Convenient synthesis of polysubstituted 3-iodofurans through the tandem ring-opening/cyclization reaction of 1-alkynyl-2,3-epoxy alcohols".SYNTHESIS-STUTTGART .21(2007):3295-3300. |
入库方式: OAI收割
来源:兰州化学物理研究所
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