C-H functionalization is a chemically challenging but highly desirable transformation. 2-oxoglutarate-dependent oxygenases (2OGXs) are remarkably versatile biocatalysts for the activation of C-H bonds. In nature, they have been shown to accept both small and large molecules carrying out a plethora of reactions, including hydroxylations, demethylations, ring formations, rearrangements, desaturations, and halogenations, making them promising candidates for industrial manufacture. In this review, we describe the current status of 2OGX use in biocatalytic applications concentrating on 2OGX-catalyzed oxyfunctionalization of amino acids and synthesis of antibiotics. Looking forward, continued bioinformatic sourcing will help identify additional, ...
Biocatalytic oxyfunctionalizations, especially of non - activated hydrocarbons, attract considerable...
As depicted in Chapter I, 2-oxoglutarate- (2OG) dependent oxygenases are ubiquitous in living system...
Modification of aliphatic C–H bonds in a regio- and stereoselective manner can pose a formidable cha...
C⁻H functionalization is a chemically challenging but highly desirable transformation. 2-oxogl...
2-Oxoglutarate (2OG)-dependent oxygenases (2OGXs) catalyze a remarkably diverse range of oxidative r...
Cytochrome P450 enzymes (P450s) are a superfamily of monooxygenase enzymes with enormous potential f...
Hydroxylases introduce hydroxyl groups with excellent regio- and enantioselectivity making them of s...
Ferrous-iron/2-oxoglutarate(2-OG)-dependent oxygenases have emerged as a widely distributed family o...
The first identfied 2-oxoglutarate (2OG) dependent oxygenase was a collagen modifying enzyme in the ...
The 2‐oxoglutarate (2OG) dependent oxygenases were first identified as having roles in the post‐tran...
The selective oxygenation of non-activated carbon atoms is an ongoing synthetic challenge and biocat...
The late-stage oxidative functionalisation of C-H bonds can be used to circumvent synthetic route re...
Selective oxidation of unactivated C–H bonds remains a central challenge in synthetic chemistry. Cyt...
Iron is an especially important redox-active cofactor in biology because of its ability to mediate r...
Members of the 2-oxoglutarate (2OG)- and Fe(II)-dependent oxygenase (2OG oxygenase) superfamily cata...
Biocatalytic oxyfunctionalizations, especially of non - activated hydrocarbons, attract considerable...
As depicted in Chapter I, 2-oxoglutarate- (2OG) dependent oxygenases are ubiquitous in living system...
Modification of aliphatic C–H bonds in a regio- and stereoselective manner can pose a formidable cha...
C⁻H functionalization is a chemically challenging but highly desirable transformation. 2-oxogl...
2-Oxoglutarate (2OG)-dependent oxygenases (2OGXs) catalyze a remarkably diverse range of oxidative r...
Cytochrome P450 enzymes (P450s) are a superfamily of monooxygenase enzymes with enormous potential f...
Hydroxylases introduce hydroxyl groups with excellent regio- and enantioselectivity making them of s...
Ferrous-iron/2-oxoglutarate(2-OG)-dependent oxygenases have emerged as a widely distributed family o...
The first identfied 2-oxoglutarate (2OG) dependent oxygenase was a collagen modifying enzyme in the ...
The 2‐oxoglutarate (2OG) dependent oxygenases were first identified as having roles in the post‐tran...
The selective oxygenation of non-activated carbon atoms is an ongoing synthetic challenge and biocat...
The late-stage oxidative functionalisation of C-H bonds can be used to circumvent synthetic route re...
Selective oxidation of unactivated C–H bonds remains a central challenge in synthetic chemistry. Cyt...
Iron is an especially important redox-active cofactor in biology because of its ability to mediate r...
Members of the 2-oxoglutarate (2OG)- and Fe(II)-dependent oxygenase (2OG oxygenase) superfamily cata...
Biocatalytic oxyfunctionalizations, especially of non - activated hydrocarbons, attract considerable...
As depicted in Chapter I, 2-oxoglutarate- (2OG) dependent oxygenases are ubiquitous in living system...
Modification of aliphatic C–H bonds in a regio- and stereoselective manner can pose a formidable cha...