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Integration of multiple active sites on large-pore mesoporous silica for enantioselective tandem reactions†
Xuelin Xia,Jingjing Meng,Hanxin Wu,Tanyu Cheng,Guohua Liu
Chemical Communications Pub Date : 01/04/2017 00:00:00 , DOI:10.1039/C6CC09008G
Abstract

Facile construction of a multifunctional heterogeneous catalyst through the assembly of Au/carbene and chiral ruthenium/diamine dual complexes in large-pore mesoporous silica was developed. This enables an efficient one-pot hydration-asymmetric transfer hydrogenation enantioselective tandem reaction of haloalkynes, affording chiral halohydrins with up to 99% enantioselectivity. Combined multifunctionalities, such as substrate-promoted silanol-functionality, BF4 anion-bonding gold/carbene and covalent-bonding chiral ruthenium/diamine active centers, contributed cooperatively to the catalytic performance.

Graphical abstract: Integration of multiple active sites on large-pore mesoporous silica for enantioselective tandem reactions
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