Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol301647g
Title: Asymmetric construction of functionalized bicyclic imides via [3 + 2] annulation of MBH carbonates catalyzed by dipeptide-based phosphines
Authors: Zhong, F.
Chen, G.-Y.
Han, X.
Yao, W.
Lu, Y. 
Issue Date: 20-Jul-2012
Citation: Zhong, F., Chen, G.-Y., Han, X., Yao, W., Lu, Y. (2012-07-20). Asymmetric construction of functionalized bicyclic imides via [3 + 2] annulation of MBH carbonates catalyzed by dipeptide-based phosphines. Organic Letters 14 (14) : 3764-3767. ScholarBank@NUS Repository. https://doi.org/10.1021/ol301647g
Abstract: A highly enantioselective [3 + 2] annulation of MBH carbonates and maleimides catalyzed by chiral phosphines has been developed. In the presence of 5 mol % of l-Thr-l-Val-derived phosphine 6, functionalized bicyclic imides were prepared in excellent yields, and with high diastereoselectivities and nearly perfect enantioselectivities. © 2012 American Chemical Society.
Source Title: Organic Letters
URI: http://scholarbank.nus.edu.sg/handle/10635/75617
ISSN: 15237060
DOI: 10.1021/ol301647g
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