中文版 | English
Title

Highly efficient and enantioselective synthesis of chiral lactones via Ir-catalysed asymmetric hydrogenation of ketoesters

Author
Corresponding AuthorChen, Gen-Qiang; Zhang, Xumu
Publication Years
2022-06-01
DOI
Source Title
ISSN
1359-7345
EISSN
1364-548X
Volume58Pages:8408-8411
Abstract
Owing to the biological significance and great synthetic value of chiral lactones and their derivatives, increasing attention has been paid to developing effective synthetic methods for chiral lactones. We herein report an efficient asymmetric hydrogenation of benzo-fused ketoesters, gamma-ketoesters and biaryl-bridged ketoesters catalyzed by chiral iridium complexes bearing ferrocene-based chiral ligands, furnishing a series of chiral lactones in superb yields and excellent enantioselectivities (up to 99% yields and up to 99% ee).
URL[Source Record]
Indexed By
SCI ; EI
Language
English
Important Publications
NI Journal Papers
SUSTech Authorship
Corresponding
Funding Project
National Natural Science Foundation of China["21901107","22171129"] ; Shenzhen Bay Laboratory[SZBL2019062801006] ; Shenzhen Science and Technology Innovation Committee["JCYJ20210324104202007","KQTD2015071710315717"] ; Key-Area Research and Development Program of Guangdong Province["2021B1111110001","2020B010188001"] ; Stable Support Plan Program of Shenzhen Natural Science Fund[20200925161222002] ; Innovative Team of Universities in Guangdong Province[2020KCXTD016] ; Guangdong Basic and Applied Basic Research Foundation[2022B1515020055]
WOS Research Area
Chemistry
WOS Subject
Chemistry, Multidisciplinary
WOS Accession No
WOS:000821433100001
Publisher
EI Accession Number
20223412623199
EI Keywords
Catalysis ; Esters ; Hydrogenation ; Iridium compounds ; Iron compounds ; Ligands ; Organometallics
ESI Classification Code
Physical Chemistry:801.4 ; Chemical Reactions:802.2 ; Organic Compounds:804.1
ESI Research Field
CHEMISTRY
Data Source
Web of Science
Citation statistics
Cited Times [WOS]:0
Document TypeJournal Article
Identifierhttp://kc.sustech.edu.cn/handle/2SGJ60CL/355869
DepartmentDepartment of Chemistry
前沿与交叉科学研究院
Affiliation
1.Harbin Inst Technol, Sch Chem & Chem Engn, Harbin 150001, Peoples R China
2.Southern Univ Sci & Technol, Dept Chem, 1088 Xueyuan Rd, Shenzhen 518055, Peoples R China
3.Shenzhen Bay Lab, Shenzhen 518132, Peoples R China
4.Southern Univ Sci & Technol, Acad Adv Interdisciplinary Studies, Dept Chem, 1088 Xueyuan Rd, Shenzhen 518055, Peoples R China
First Author AffilicationDepartment of Chemistry
Corresponding Author AffilicationDepartment of Chemistry;  Academy for Advanced Interdisciplinary Studies
Recommended Citation
GB/T 7714
Song, Jingyuan,Yin, Congcong,Zhang, Yao,et al. Highly efficient and enantioselective synthesis of chiral lactones via Ir-catalysed asymmetric hydrogenation of ketoesters[J]. CHEMICAL COMMUNICATIONS,2022,58:8408-8411.
APA
Song, Jingyuan.,Yin, Congcong.,Zhang, Yao.,Shi, Yongjie.,Li, Yingjun.,...&Zhang, Xumu.(2022).Highly efficient and enantioselective synthesis of chiral lactones via Ir-catalysed asymmetric hydrogenation of ketoesters.CHEMICAL COMMUNICATIONS,58,8408-8411.
MLA
Song, Jingyuan,et al."Highly efficient and enantioselective synthesis of chiral lactones via Ir-catalysed asymmetric hydrogenation of ketoesters".CHEMICAL COMMUNICATIONS 58(2022):8408-8411.
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