Regioselective C─H Functionalization by the Combination of Enzymatic and Chemocatalytic Reactions in Water
Ran Zhu1,2, Xuhua Mo3, Tanja Gulder4,5
1Chair of Technical Biochemistry, Department of Chemistry and Food Chemistry, Technical University of Dresden, Bergstraße 66, Dresden, 01069, Germany.
Abstract:
The combination of bio- and chemo-catalytic processes has tremendous potential for the sustainable production of important synthetic building blocks. Such approaches capitalize on the often-high selectivity of enzymes and the broad arsenal of synthetic transformations to access highly functionalized molecules from simple precursors. However, the strict requirement of enzymes for an aqueous reaction environment, often combined with their lack of stability under harsh reaction conditions, makes the development of efficient chemo-enzymatic cascade reactions challenging. Within this work, we developed a chemo-enzymatic platform that combines regioselective enzymatic Halogenation, chemo-catalytic Heck coupling, and an enzyme-catalyzed Hydrolysis reaction (H3 Catalytic Platform = H3CP) in a single reaction vessel. H3CP uses water as a reaction solvent to facilitate the enzymatic transformations, with the cross-coupling reaction taking place in dynamic and protective super-molecular reaction vessels composed of the commercially available TPGS-705-M. Our work utilizes various halogenating enzymes (FDHs and VHPOs), selectively functionalizing diverse substrates, thus enabling subsequent metal-catalyzed cross-coupling followed by enzymatic hydrolysis. H3CP gives access to a broad range of valuable acrylic acid building blocks with diverse functionalization at the aromatic portion.
More Related Videos
05:34Efficient Synthesis of Polyfunctionalized Benzenes in Water via Persulfate-promoted Benzannulation of α,β-Unsaturated Compounds and Alkynes
Published on: December 16, 2019
10:39Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction
Published on: August 23, 2018
Related Concept Videos
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Regioselectivity of Electrophilic Additions to Alkenes: Markovnikov's Rule
The hydrohalogenation of an unsymmetrical alkene can yield two haloalkane products, depending on which vinylic carbon takes up the halogen. However, one product usually predominates, where hydrogen adds to the vinylic carbon bearing the...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Regioselectivity of Electrophilic Additions-Peroxide Effect
Regioselective Formation of Enolates
