Organic chemistry, Stereochemistry, Catalysis, Enzyme and Biocatalysis are his primary areas of study. Marko D. Mihovilovic has included themes like Cyclohexanone monooxygenase, Yeast, Escherichia coli, Phenylacetone monooxygenase and Baeyer–Villiger oxidation in his Stereochemistry study. His Phenylacetone monooxygenase research is multidisciplinary, relying on both Cofactor and Enantioselective synthesis.
His Baeyer–Villiger oxidation research includes themes of Directed evolution and Recombinant DNA. His Catalysis study combines topics from a wide range of disciplines, such as Substrate, Aryl, Tandem and Surface modification. His Biocatalysis study integrates concerns from other disciplines, such as Bioorganic chemistry, Chemical space, Protein sequencing and High selectivity.
Marko D. Mihovilovic spends much of his time researching Stereochemistry, Organic chemistry, Catalysis, Combinatorial chemistry and Biocatalysis. His Stereochemistry study incorporates themes from Recombinant DNA, Escherichia coli, Substrate, Enzyme and Baeyer–Villiger oxidation. His studies deal with areas such as Ketone, Bicyclic molecule and Biotransformation as well as Baeyer–Villiger oxidation.
His work in Enantioselective synthesis, Solvent, Regioselectivity, Kinetic resolution and Furan are all subfields of Organic chemistry research. His Catalysis research is multidisciplinary, incorporating perspectives in Surface modification, Pyridine, Medicinal chemistry and Aryl. Marko D. Mihovilovic interconnects Enantiomeric excess and Stereoselectivity in the investigation of issues within Biocatalysis.
Marko D. Mihovilovic mainly focuses on Stereochemistry, Combinatorial chemistry, Organic chemistry, Substrate and GABAA receptor. His work deals with themes such as Biocatalysis, Enantioselective synthesis, Regioselectivity, Enzyme and Stereoselectivity, which intersect with Stereochemistry. His research investigates the connection with Enzyme and areas like Aryl which intersect with concerns in Moiety.
He has researched Combinatorial chemistry in several fields, including Catalysis and Metal. His work on Organic chemistry deals in particular with Solvent, Aldol reaction and Aldehyde. His biological study spans a wide range of topics, including In vivo, Chemical engineering and High Throughput Assay.
Marko D. Mihovilovic mainly investigates Stereochemistry, Pharmacology, Biochemistry, Receptor and Combinatorial chemistry. His Stereochemistry research includes elements of Biocatalysis, Chloride channel, Organic chemistry and Desymmetrization. His research on Organic chemistry frequently connects to adjacent areas such as Cascade.
Many of his research projects under Biochemistry are closely connected to Carboxylate reductase activity with Carboxylate reductase activity, tying the diverse disciplines of science together. His Combinatorial chemistry study combines topics in areas such as Reagent, Metal and Catalysis. Marko D. Mihovilovic works mostly in the field of Baeyer–Villiger oxidation, limiting it down to topics relating to Enantioselective synthesis and, in certain cases, Substrate, as a part of the same area of interest.
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Discovery and resupply of pharmacologically active plant-derived natural products: A review.
Atanas G. Atanasov;Birgit Waltenberger;Eva-Maria Pferschy-Wenzig;Thomas Linder.
Biotechnology Advances (2015)
Opportunities and challenges for combining chemo- and biocatalysis
Florian Rudroff;Marko D. Mihovilovic;Harald Gröger;Radka Snajdrova.
Nature Catalysis (2018)
Monooxygenase‐Mediated Baeyer−Villiger Oxidations
Marko D. Mihovilovic;Bernhard Müller;Peter Stanetty.
European Journal of Organic Chemistry (2002)
Cascade catalysis – strategies and challenges en route to preparative synthetic biology
Jan Muschiol;Christin Peters;Nikolin Oberleitner;Marko D. Mihovilovic.
Chemical Communications (2015)
Cross-Coupling Reactions on Azoles with Two and More Heteroatoms
Michael Schnürch;Radoslav Flasik;Ather Farooq Khan;Markus Spina.
European Journal of Organic Chemistry (2006)
Facile, solvent and ligand free iron catalyzed direct functionalization of N-protected tetrahydroisoquinolines and isochroman.
Michael Ghobrial;Karin Harhammer;Marko D. Mihovilovic;Michael Schnürch.
Chemical Communications (2010)
Recent Developments in the Application of Baeyer–Villiger Monooxygenases as Biocatalysts
Gonzalo de Gonzalo;Marko D. Mihovilovic;Marco W. Fraaije.
Enzyme Mediated Baeyer-Villiger Oxidations
Marko D. Mihovilovic.
Current Organic Chemistry (2006)
Halogen dance reactions—A review
Michael Schnürch;Markus Spina;Ather Farooq Khan;Marko D. Mihovilovic.
Chemical Society Reviews (2007)
Direct Functionalization of (Un)protected Tetrahydroisoquinoline and Isochroman under Iron and Copper Catalysis: Two Metals, Two Mechanisms
Michael Ghobrial;Michael Schnürch;Marko D. Mihovilovic.
Journal of Organic Chemistry (2011)
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