Guanidine-catalyzed enantioselective desymmetrization of meso-aziridines
Type
ArticleAuthors
Zhang, YanKee, Choonwee
Lee, Richmond
Fu, Xiao
Soh, J. Y T
Loh, E. M F
Huang, Kuo-Wei

Tan, Choonhong
KAUST Department
Biological and Environmental Sciences and Engineering (BESE) DivisionChemical Science Program
Homogeneous Catalysis Laboratory (HCL)
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division
Date
2011Permanent link to this record
http://hdl.handle.net/10754/561648
Metadata
Show full item recordAbstract
An amino-indanol derived chiral guanidine was developed as an efficient Brønsted base catalyst for the desymmetrization of meso-aziridines with both thiols and carbamodithioic acids as nucleophiles, which provided 1,2-difunctionalized ring-opened products in high yields and enantioselectivities. © The Royal Society of Chemistry.Citation
Zhang, Y., Kee, C. W., Lee, R., Fu, X., Soh, J. Y.-T., Loh, E. M. F., … Tan, C.-H. (2011). Guanidine-catalyzed enantioselective desymmetrization of meso-aziridines. Chemical Communications, 47(13), 3897. doi:10.1039/c0cc05840hPublisher
Royal Society of Chemistry (RSC)Journal
Chemical CommunicationsPubMed ID
21336394Relations
Is Supplemented By:- [Dataset]
Zhang, Y., Kee, C. W., Lee, R., Fu, X., Soh, J. Y.-T., Loh, E. M. F., … Tan, C.-H. (2011). CCDC 806368: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/ccw22ww. DOI: 10.5517/ccw22ww HANDLE: 10754/624627 - [Dataset]
Zhang, Y., Kee, C. W., Lee, R., Fu, X., Soh, J. Y.-T., Loh, E. M. F., … Tan, C.-H. (2011). CCDC 806369: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/ccw22xx. DOI: 10.5517/ccw22xx HANDLE: 10754/624628
ae974a485f413a2113503eed53cd6c53
10.1039/c0cc05840h
Scopus Count
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