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A noncovalent hybrid of [Pd(phen)(OAc)2] and st-DNA for the enantioselective hydroamination of β-nitrostyrene with methoxyamine†‡
Mrityunjoy Pal,Dulal Musib,Maynak Pal,Gopal Rana,Gobinda Bag,Subrata Dutta,Mithun Roy
Organic & Biomolecular Chemistry Pub Date : 05/13/2021 00:00:00 , DOI:10.1039/D1OB00714A
Abstract

We developed a novel Pd-catalysed enantioselective synthesis of C–N bonds using the chiral scaffold of DNA. The non-covalently linked [Pd(phen)(OAc)2] with st-DNA catalysed the Markonicov hydroamination of β-nitrostyrene with methoxyamine for the first time with >75% enantiomeric excess (ee) in an aqueous buffer (pH 7.4) at room temperature.

Graphical abstract: A noncovalent hybrid of [Pd(phen)(OAc)2] and st-DNA for the enantioselective hydroamination of β-nitrostyrene with methoxyamine
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