Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/35780
Title: Highly enantioselective ring-opening reactions of Aziridines with Indole and its application in the building of C-3-Halogenated Pyrroloindolines
Authors: Yang, DX
Wang, LQ
Han, FX
Li, D
Zhao, DP
Cao, YM
Ma, YX
Kong, WD
Sun, QT
Wang, R
Keywords: Asymmetric synthesis
Cyclization
Magnesium
Ring-opening reactions
Issue Date: 2014
Publisher: Wiley-VCH
Source: Chemistry - a European journal, 2014, v. 20, no. 50, p. 16478-16483 How to cite?
Journal: Chemistry - a European journal 
Abstract: A magnesium-catalyzed asymmetric ring-opening reaction of aziridine with indole has been realized by employing commercially available chiral ligands. Both of the enantiomers of the ring-opening product could be obtained with good yields and a high level of enantioselectivity. The corresponding ring-opening product could be further transformed to various types of enantioenriched C-3-halogenated-pyrroloindolines.
URI: http://hdl.handle.net/10397/35780
ISSN: 0947-6539 (print)
1521-3765 (online)
DOI: 10.1002/chem.201404354
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