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Iron-catalyzed tetrasubstituted alkene formation from alkynes and sodium sultinates
Liu, Saiwen1; Tang, Lichang1; Chen, Hui1; Zhao, Feng1; Deng, Guo-Jun1,2
刊名ORGANIC & BIOMOLECULAR CHEMISTRY
2014-08-28
卷号12期号:32页码:6076-6079
ISSN号1477-0520
DOI10.1039/c4ob00816b
英文摘要An iron-catalyzed sulfenylation and arylation of alkynes with aryl sulfinic acid sodium salts is described. Various aromatic sodium sulfinates acted both as aryl and sulfenylation reagents, affording tetrasubstituted alkenes in one pot with good yields.
语种英语
出版者ROYAL SOC CHEMISTRY
WOS记录号WOS:000340352700006
内容类型期刊论文
源URL[http://ir.iccas.ac.cn/handle/121111/50159]  
专题中国科学院化学研究所
通讯作者Deng, Guo-Jun
作者单位1.Xiangtan Univ, Key Lab Environm Friendly Chem & Applicat, Minist Educ, Coll Chem, Xiangtan 411105, Peoples R China
2.Chinese Acad Sci, Inst Chem, Key Lab Mol Recognit & Funct, Beijing 100080, Peoples R China
推荐引用方式
GB/T 7714
Liu, Saiwen,Tang, Lichang,Chen, Hui,et al. Iron-catalyzed tetrasubstituted alkene formation from alkynes and sodium sultinates[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2014,12(32):6076-6079.
APA Liu, Saiwen,Tang, Lichang,Chen, Hui,Zhao, Feng,&Deng, Guo-Jun.(2014).Iron-catalyzed tetrasubstituted alkene formation from alkynes and sodium sultinates.ORGANIC & BIOMOLECULAR CHEMISTRY,12(32),6076-6079.
MLA Liu, Saiwen,et al."Iron-catalyzed tetrasubstituted alkene formation from alkynes and sodium sultinates".ORGANIC & BIOMOLECULAR CHEMISTRY 12.32(2014):6076-6079.
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