Recent Advances in Iron Catalysis
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 catal...
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| Format: | Book Chapter |
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Basel, Switzerland
MDPI - Multidisciplinary Digital Publishing Institute
2020
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| Online Access: | Get Fullteks DOAB: description of the publication |
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| LEADER | 04308naaaa2201009uu 4500 | ||
|---|---|---|---|
| 001 | doab_20_500_12854_69132 | ||
| 005 | 20210501 | ||
| 020 | |a books978-3-03943-119-9 | ||
| 020 | |a 9783039431182 | ||
| 020 | |a 9783039431199 | ||
| 024 | 7 | |a 10.3390/books978-3-03943-119-9 |c doi | |
| 041 | 0 | |a English | |
| 042 | |a dc | ||
| 072 | 7 | |a GP |2 bicssc | |
| 100 | 1 | |a Knölker, Hans-Joachim |4 edt | |
| 700 | 1 | |a Knölker, Hans-Joachim |4 oth | |
| 245 | 1 | 0 | |a Recent Advances in Iron Catalysis |
| 260 | |a Basel, Switzerland |b MDPI - Multidisciplinary Digital Publishing Institute |c 2020 | ||
| 300 | |a 1 electronic resource (224 p.) | ||
| 506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
| 520 | |a 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. | ||
| 540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |4 https://creativecommons.org/licenses/by/4.0/ | ||
| 546 | |a English | ||
| 650 | 7 | |a Research & information: general |2 bicssc | |
| 653 | |a iron | ||
| 653 | |a cross-coupling | ||
| 653 | |a aryl esters | ||
| 653 | |a C-O activation | ||
| 653 | |a Fe-catalysis | ||
| 653 | |a Kumada cross-coupling | ||
| 653 | |a iron complexes | ||
| 653 | |a hydrogen transfer | ||
| 653 | |a reductive amination | ||
| 653 | |a alcohols | ||
| 653 | |a amines | ||
| 653 | |a decarbonylation | ||
| 653 | |a alkylation | ||
| 653 | |a spirocyclization | ||
| 653 | |a aldehyde | ||
| 653 | |a cinnamamide | ||
| 653 | |a iron catalysis | ||
| 653 | |a bis-(aryl)manganese | ||
| 653 | |a alkenyl halides | ||
| 653 | |a ate iron(II) complex | ||
| 653 | |a asymmetric catalysis | ||
| 653 | |a nitrogen ligand | ||
| 653 | |a oxidative coupling | ||
| 653 | |a BINOL synthesis | ||
| 653 | |a carbene | ||
| 653 | |a diazoalkane | ||
| 653 | |a C-H functionalization | ||
| 653 | |a catalysis | ||
| 653 | |a borylation | ||
| 653 | |a Iron | ||
| 653 | |a C-H functionalisation | ||
| 653 | |a pinacolborane | ||
| 653 | |a photochemistry | ||
| 653 | |a amidation | ||
| 653 | |a iron(III) chloride | ||
| 653 | |a amides | ||
| 653 | |a esters | ||
| 653 | |a solvent-free | ||
| 653 | |a iron-catalysis | ||
| 653 | |a carboazidation | ||
| 653 | |a β-methyl scission | ||
| 653 | |a radical | ||
| 653 | |a DFT | ||
| 653 | |a organic synthesis | ||
| 653 | |a C-H activation | ||
| 653 | |a C-C coupling | ||
| 653 | |a α-alkenylation | ||
| 653 | |a dehydrogenative coupling | ||
| 653 | |a sustainability | ||
| 653 | |a naphthidines | ||
| 653 | |a fluorescence | ||
| 653 | |a iron catalyst | ||
| 653 | |a ATRP | ||
| 653 | |a controlled radical polymerization | ||
| 653 | |a external stimuli | ||
| 653 | |a asymmetric transfer hydrogenation | ||
| 653 | |a density functional theory | ||
| 653 | |a bifunctional catalyst | ||
| 653 | |a haloalkane coupling | ||
| 653 | |a Grignard reagent | ||
| 653 | |a FeI/FeII/FeIII mechanism | ||
| 856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/2904 |7 0 |z Get Fullteks |
| 856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/69132 |7 0 |z DOAB: description of the publication |