中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Bifunctional Ligand Enables Efficient Gold-Catalyzed Hydroalkenylation of Propargylic Alcohol

文献类型:期刊论文

作者Cheng, XP; Liao, SR; Porta, A; Ma, X; Zanoni, G; Zhang, LM
刊名ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
出版日期2018
卷号57期号:27页码:8250-8254
通讯作者gz@unipv.it ; zhang@chem.ucsb.edu
英文摘要Using the previously designed biphenyl-2-ylphosphine ligand, featuring a remote tertiary amino group, the first gold-catalyzed intermolecular hydroalkenylation of alkynes has been developed. Synthetically valuable conjugated dienyl alcohols are formed in moderate to good yields. A range of alkenyltrifluoroborates are allowed as the alkenyl donor, and no erosion of alkene geometry and/or the propargylic configuration are detected. DFT calculations confirm the critical role of the remote basic group in the ligand as a general-base catalyst for promoting this novel gold catalysis with good efficiency.
学科主题Chemistry
关键词[WOS]conjugation ; gold ; ligand design ; reaction mechanisms ; synthetic methods
源URL[http://ir.scsio.ac.cn/handle/344004/16923]  
专题南海海洋研究所_中科院海洋生物资源可持续利用重点实验室
推荐引用方式
GB/T 7714
Cheng, XP,Liao, SR,Porta, A,et al. Bifunctional Ligand Enables Efficient Gold-Catalyzed Hydroalkenylation of Propargylic Alcohol[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,2018,57(27):8250-8254.
APA Cheng, XP,Liao, SR,Porta, A,Ma, X,Zanoni, G,&Zhang, LM.(2018).Bifunctional Ligand Enables Efficient Gold-Catalyzed Hydroalkenylation of Propargylic Alcohol.ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,57(27),8250-8254.
MLA Cheng, XP,et al."Bifunctional Ligand Enables Efficient Gold-Catalyzed Hydroalkenylation of Propargylic Alcohol".ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 57.27(2018):8250-8254.

入库方式: OAI收割

来源:南海海洋研究所

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