A palladium-catalyzed enantioselective hydroesterification of alkenylphenols with phenyl formate. A facile approach to optically active dihydrocoumarins
Li, Jingfu1; Chang, Wenju1; Ren, Wenlong1; Liu, Wei1; Wang, Haining1; Shi, Yian1,2,3
刊名ORGANIC & BIOMOLECULAR CHEMISTRY
2015
卷号13期号:41页码:10341-10347
英文摘要An effective palladium-catalyzed enantioselective hydroesterification of alkenylphenols with phenyl formate as a CO source is described. A variety of optically active dihydrocoumarins can be obtained in generally high yields with up to 91% ee.
收录类别SCI
语种英语
公开日期2015-12-22
内容类型期刊论文
源URL[http://ir.iccas.ac.cn/handle/121111/29153]  
专题化学研究所_分子识别与功能实验室
作者单位1.Nanjing Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Chem Life Sci, Ctr Multimol Organ Chem,State Key Lab Coordinat C, Nanjing 210093, Jiangsu, Peoples R China
2.Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
3.Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
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GB/T 7714
Li, Jingfu,Chang, Wenju,Ren, Wenlong,et al. A palladium-catalyzed enantioselective hydroesterification of alkenylphenols with phenyl formate. A facile approach to optically active dihydrocoumarins[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2015,13(41):10341-10347.
APA Li, Jingfu,Chang, Wenju,Ren, Wenlong,Liu, Wei,Wang, Haining,&Shi, Yian.(2015).A palladium-catalyzed enantioselective hydroesterification of alkenylphenols with phenyl formate. A facile approach to optically active dihydrocoumarins.ORGANIC & BIOMOLECULAR CHEMISTRY,13(41),10341-10347.
MLA Li, Jingfu,et al."A palladium-catalyzed enantioselective hydroesterification of alkenylphenols with phenyl formate. A facile approach to optically active dihydrocoumarins".ORGANIC & BIOMOLECULAR CHEMISTRY 13.41(2015):10341-10347.
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