Please use this identifier to cite or link to this item: https://doi.org/10.1039/c2cc16904e
Title: Asymmetric [3+2] annulation of allenes with maleimides catalyzed by dipeptide-derived phosphines: Facile creation of functionalized bicyclic cyclopentenes containing two tertiary stereogenic centers
Authors: Zhao, Q.
Han, X.
Wei, Y.
Shi, M.
Lu, Y. 
Issue Date: 25-Jan-2012
Source: Zhao, Q., Han, X., Wei, Y., Shi, M., Lu, Y. (2012-01-25). Asymmetric [3+2] annulation of allenes with maleimides catalyzed by dipeptide-derived phosphines: Facile creation of functionalized bicyclic cyclopentenes containing two tertiary stereogenic centers. Chemical Communications 48 (7) : 970-972. ScholarBank@NUS Repository. https://doi.org/10.1039/c2cc16904e
Abstract: d-Threonine-l-tert-leucine-derived bifunctional phosphine, Cat. 11, catalyzed highly enantioselective [3+2] annulation of maleimides with allenes has been disclosed, allowing the synthesis of optically active functionalized bicyclic cyclopentenes containing two tertiary stereogenic centers in good to high yields along with good to high enantioselectivities. © 2012 The Royal Society of Chemistry.
Source Title: Chemical Communications
URI: http://scholarbank.nus.edu.sg/handle/10635/75612
ISSN: 13597345
DOI: 10.1039/c2cc16904e
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