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|Title:||Asymmetric construction of functionalized bicyclic imides via [3 + 2] annulation of MBH carbonates catalyzed by dipeptide-based phosphines||Authors:||Zhong, F.
|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|
|Appears in Collections:||Staff Publications|
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