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Biocatalysis, that is, the use of biological catalysts (enzymes, cells, etc.) for the preparation of highly valuable compounds is undergoing a great development, being considered an extremely sustainable approach to undertaking environmental demands. In this scenario, this book illustrates the versatility of applied biocatalysis for the preparation of drugs and other bioactive compounds through the presentation of different research articles and reviews, in which several authors describe the most recent developments in this appealing scientific area. By reading the excellent contributions gathered in this book, it is possible to have an updated idea about new advances and possibilities for a new exciting future.

n/a --- biotransformations --- glycosidases --- bacteria --- OcUGT1 --- antioxidant activity --- glycodiverfication --- benzoxathiepins --- coprostanol --- 7-methylguanosine iodide --- sulfuretin --- chondroitin sulfates --- 7-methylguanine arabinoside iodide --- 7-methyl-2?-deoxyguanosine iodide --- microalgae --- chitosan oligosaccharides --- deacetylation degree --- cholesterol --- Tecadenoson --- esterase --- metabolic pathways --- chitinases --- alcohol --- transglycosylation reaction --- MALDI-TOF --- photooxidation --- aqueous solubility --- ?-transaminase --- cascade --- nutraceutical --- antimuscarinic agents --- extraction --- rutin oligomers --- Alcalase® --- HPSEC --- Cladribine --- purine nucleoside phosphorylase --- pleiotropic effects --- biotransamination --- amino acid --- stereoselective --- laccase activity --- biocatalysis --- Ribavirin --- lyases --- chitosanases --- anti-inflammatory --- glycosaminoglycan --- polysaccharides --- amine transaminases --- ester hydrolysis --- Spirulina --- asymmetric synthesis --- reductive amination --- glycosyltransferase --- statins --- stereoselective synthesis --- xanthine oxidase inhibition --- reduction reaction --- pig liver esterase (PLE)

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Transition metal-catalyzed reactions play a key role in many transformations of synthetic organic chemistry. For most of these reactions, noble metals, for example, palladium, have been used as catalysts. Over the last two decades, more and more first row transition metals have been applied as catalysts for organic reactions, with iron taking the center stage. The driving forces behind this development are not only the high costs for the noble metals but also their toxicity. Iron is the most abundant transition metal in the Earth’s crust, and thus, it is considerably cheaper than the precious noble metals. Moreover, iron compounds are involved in many biological processes, and thus, iron exhibits a low toxicity. Because of this low toxicity, iron-catalyzed reactions are important for an environmentally benign sustainable chemistry. However, iron catalysts are not only investigated to replace noble metals; they offer many applications in synthesis beyond those of classical noble metal catalysts. Several articles of the present book emphasize the complementarity of iron-catalyzed reactions as compared to reactions catalyzed by noble metals. The book shows intriguing recent developments and the current standing of iron-catalyzed reactions as well as applications to organic synthesis.

Research & information: general --- iron --- cross-coupling --- aryl esters --- C–O activation --- Fe-catalysis --- Kumada cross-coupling --- iron complexes --- hydrogen transfer --- reductive amination --- alcohols --- amines --- decarbonylation --- alkylation --- spirocyclization --- aldehyde --- cinnamamide --- iron catalysis --- bis-(aryl)manganese --- alkenyl halides --- ate iron(II) complex --- asymmetric catalysis --- nitrogen ligand --- oxidative coupling --- BINOL synthesis --- carbene --- diazoalkane --- C-H functionalization --- catalysis --- borylation --- Iron --- C-H functionalisation --- pinacolborane --- photochemistry --- amidation --- iron(III) chloride --- amides --- esters --- solvent-free --- iron-catalysis --- carboazidation --- β-methyl scission --- radical --- DFT --- organic synthesis --- C-H activation --- C-C coupling --- α-alkenylation --- dehydrogenative coupling --- sustainability --- naphthidines --- fluorescence --- iron catalyst --- ATRP --- controlled radical polymerization --- external stimuli --- asymmetric transfer hydrogenation --- density functional theory --- bifunctional catalyst --- haloalkane coupling --- Grignard reagent --- FeI/FeII/FeIII mechanism --- iron --- cross-coupling --- aryl esters --- C–O activation --- Fe-catalysis --- Kumada cross-coupling --- iron complexes --- hydrogen transfer --- reductive amination --- alcohols --- amines --- decarbonylation --- alkylation --- spirocyclization --- aldehyde --- cinnamamide --- iron catalysis --- bis-(aryl)manganese --- alkenyl halides --- ate iron(II) complex --- asymmetric catalysis --- nitrogen ligand --- oxidative coupling --- BINOL synthesis --- carbene --- diazoalkane --- C-H functionalization --- catalysis --- borylation --- Iron --- C-H functionalisation --- pinacolborane --- photochemistry --- amidation --- iron(III) chloride --- amides --- esters --- solvent-free --- iron-catalysis --- carboazidation --- β-methyl scission --- radical --- DFT --- organic synthesis --- C-H activation --- C-C coupling --- α-alkenylation --- dehydrogenative coupling --- sustainability --- naphthidines --- fluorescence --- iron catalyst --- ATRP --- controlled radical polymerization --- external stimuli --- asymmetric transfer hydrogenation --- density functional theory --- bifunctional catalyst --- haloalkane coupling --- Grignard reagent --- FeI/FeII/FeIII mechanism