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A Palladium-Catalyzed Regioselective Hydroesterification of Alkenylphenols to Lactones with Phenyl Formate as CO Source
Wang, Haining1; Dong, Ben1; Wang, Yang1; Li, Jingfu1; Shi, Yian1,2,3
刊名ORGANIC LETTERS
2014-01-03
卷号16期号:1页码:186-189
ISSN号1523-7060
DOI10.1021/ol403171p
英文摘要An effective Pd(OAc)(2)-PPh3 catalyzed hydroesterification of alkenylphenols with phenyl formate as CO surrogate is described. A variety of lactones are obtained in generally high yields with high regioselectivities. In one case, 76% ee is obtained with a chiral ligand.
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:000329472800048
内容类型期刊论文
源URL[http://ir.iccas.ac.cn/handle/121111/51031]  
专题中国科学院化学研究所
通讯作者Shi, Yian
作者单位1.Nanjing Univ, Sch Chem & Chem Engn, Ctr Multimol Organ Chem, State Key Lab Coordinat Chem, 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
推荐引用方式
GB/T 7714
Wang, Haining,Dong, Ben,Wang, Yang,et al. A Palladium-Catalyzed Regioselective Hydroesterification of Alkenylphenols to Lactones with Phenyl Formate as CO Source[J]. ORGANIC LETTERS,2014,16(1):186-189.
APA Wang, Haining,Dong, Ben,Wang, Yang,Li, Jingfu,&Shi, Yian.(2014).A Palladium-Catalyzed Regioselective Hydroesterification of Alkenylphenols to Lactones with Phenyl Formate as CO Source.ORGANIC LETTERS,16(1),186-189.
MLA Wang, Haining,et al."A Palladium-Catalyzed Regioselective Hydroesterification of Alkenylphenols to Lactones with Phenyl Formate as CO Source".ORGANIC LETTERS 16.1(2014):186-189.
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