@article {35376,
	title = {Non-Covalent Immobilization of Rare Earth Heterobimetallic Frameworks and their Reactivity in an Asymmetric Michael Addition},
	journal = {Advanced Synthesis \&amp; CatalysisAdvanced Synthesis \&amp; Catalysis},
	volume = {356},
	number = {6},
	year = {2014},
	note = {Ae8hwTimes Cited:1Cited References Count:99},
	month = {Apr 14},
	pages = {1243-1254},
	abstract = {Heterobimetallic Lewis acid catalysts are broadly useful and methods to recycle them have immediate applications. However, their immobilization through covalent binding can be challenging. Non-covalent immobilization of supported asymmetric catalysts is attractive due to ease of preparation and potential for reversible binding. We report a novel non-covalent binding strategy for Shibasaki\&$\#$039;s REMB framework {RE=rare earth metal; M=Li, Na, K; B=BINOL; RE:M:B=1:3:3, [M-3(sol)(n)][(BINOLate)(3)RE]} and explore the reactivity of the supported catalyst.},
	keywords = {alpha,beta-unsaturated ketones, asymmetric catalysis, chiral lanthanide complexes, continuous-flow, convey asymmetry, enantioselective epoxidation, heterobimetallic complexes, michael addition, nitroaldol reaction, organic-synthesis, rare earths, ring-opening reactions, solid-phase synthesis, substrate-binding, supported catalysts},
	isbn = {1615-4150},
	author = {Robinson, J. R. and Yadav, J. and Fan, X. Y. and Stanton, G. R. and Schelter, E. J. and Pericas, M. A. and Walsh, P. J.}
}
