ICCAS OpenIR
Highly diastereo- and enantioselective NHC-catalyzed [3+2] annulation of enals and isatins
Sun, Li-Hui; Shen, Li-Tao; Ye, Song
2011
Source PublicationCHEMICAL COMMUNICATIONS
ISSN1359-7345
Volume47Issue:36Pages:10136-10138
AbstractThe chiral N-heterocyclic carbene bearing a proximal hydroxy group derived from L-pyroglutamic acid was found to be an efficient catalyst for the [3+2] annulation of enals and isatins to give the corresponding spirocyclic oxindolo-gamma-butyrolactones in good yield with good diastereo- and enantioselectivities.
DOI10.1039/c1cc13860j
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000294433900054
PublisherROYAL SOC CHEMISTRY
Citation statistics
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/71344
Collection中国科学院化学研究所
Corresponding AuthorYe, Song
AffiliationChinese Acad Sci, Key Lab Mol Recognit & Funct, Inst Chem, Beijing 100190, Peoples R China
Recommended Citation
GB/T 7714
Sun, Li-Hui,Shen, Li-Tao,Ye, Song. Highly diastereo- and enantioselective NHC-catalyzed [3+2] annulation of enals and isatins[J]. CHEMICAL COMMUNICATIONS,2011,47(36):10136-10138.
APA Sun, Li-Hui,Shen, Li-Tao,&Ye, Song.(2011).Highly diastereo- and enantioselective NHC-catalyzed [3+2] annulation of enals and isatins.CHEMICAL COMMUNICATIONS,47(36),10136-10138.
MLA Sun, Li-Hui,et al."Highly diastereo- and enantioselective NHC-catalyzed [3+2] annulation of enals and isatins".CHEMICAL COMMUNICATIONS 47.36(2011):10136-10138.
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