A chiral zeolite material with improved enantioselective catalytic properties prepared from readily accessible ephedrine alkaloids

Substituted-benzyl-containing N-methyl-ephedrinium derivatives (BMEP), prepared from the highly -accessible (1 R ,2 S )- or (1 S ,2 R )-ephedrine alkaloids, have been found to act as efficient structure -directing agents for the synthesis of chiral zeolite GTM-4 with -ITV framework structure, promoting the enantio-enrichment in one of the chiral crystalline polymorphs as a function of the organic handedness. Results of a systematic variation of substituents in the benzyl ring attached to the ephedrine core (with methyl-, fluoro- or chloro-groups in the different positions of the aromatic ring) revealed that F -containing SDAs brought about an improvement in the structure -directing ability toward the -ITV framework, giving asymmetric zeolite acid -catalysts that yielded notable enantiomeric excesses in the range of 40 -45 % for the trans -stilbene oxide ring -opening with 1-butanol. Interestingly, the incorporation of a methyl group in ortho-position (oMBMEP) had a double positive effect: on the one hand, this SDA prevented the crystallization of the competing BEC phase, allowing the crystallization of the -ITV structure at higher temperature and with higher crystallinity, and on the other, it drove to GTM-4 asymmetric catalysts that yielded enantiomeric excesses up to 60 %, resulting in the chiral GTM catalysts with the best enantioselective properties found so far. Remarkably, our catalytic results show the same chiral activity (in terms of zeolite handedness) for GTM-4 materials prepared from benzyl-containing (1 S ,2 S )-N-methyl- pseudoephedrinium (BMPS) and (1 S ,2 R )-N-methyl-ephedrinium (BMEP) derivatives, thus suggesting that the host -guest transfer of chirality during crystallization with these chiral organic aromatic agents is imposed by the absolute configuration of the C1 atom to which the OH group is attached. The relatively high enantiomeric excess of 60 % achieved, combined with the high accessibility of the ephedrine chiral precursors used for the synthesis that enables the production of both crystalline handedness of the -ITV framework, bring these materials closer to a potential application as heterogeneous asymmetric catalysts for the synthesis of chiral compounds of interest.