Journal
INORGANIC CHEMISTRY
Volume 57, Issue 16, Pages 9786-9789Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.8b01630
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Funding
- National Natural Science Foundation of China [21522104, 21431004, 21620102001]
- National Key Basic Research Program of China [2016YFA0203400]
- Key Project of Basic Research of Shanghai [17JC1403100, 18JC1413200]
- Shanghai Eastern Scholar Program
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A chiral porous metal organic framework (MOF) decorated with radicals has been successfully constructed by cocrystallizing achiral (2,2,6,6-tetramethyl-piperidin-1-yl)oxyl (TEMPO)-substituted tricarboxylate and enantiopure VO(salen)-derived dipyridine ligands. The chiral MOF can function as an efficient heterogeneous catalyst for the sequential alcohol oxidation/asymmetric cyanation of aldehyde reactions with enhanced activity and enantioselectivity compared to the homogeneous counterpart.
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