中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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
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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