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...

Full description

Saved in:
Bibliographic Details
Sonstige:
Year of Publication:2020
Language:English
Physical Description:1 electronic resource (224 p.)
Tags: Add Tag
No Tags, Be the first to tag this record!
id 993546078104498
ctrlnum (CKB)5400000000044046
(oapen)https://directory.doabooks.org/handle/20.500.12854/69132
(EXLCZ)995400000000044046
collection bib_alma
record_format marc
spelling Knölker, Hans-Joachim edt
Recent Advances in Iron Catalysis
Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2020
1 electronic resource (224 p.)
text txt rdacontent
computer c rdamedia
online resource cr rdacarrier
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.
English
Research & information: general bicssc
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
3-03943-118-8
3-03943-119-6
Knölker, Hans-Joachim oth
language English
format eBook
author2 Knölker, Hans-Joachim
author_facet Knölker, Hans-Joachim
author2_variant h j k hjk
author2_role Sonstige
title Recent Advances in Iron Catalysis
spellingShingle Recent Advances in Iron Catalysis
title_full Recent Advances in Iron Catalysis
title_fullStr Recent Advances in Iron Catalysis
title_full_unstemmed Recent Advances in Iron Catalysis
title_auth Recent Advances in Iron Catalysis
title_new Recent Advances in Iron Catalysis
title_sort recent advances in iron catalysis
publisher MDPI - Multidisciplinary Digital Publishing Institute
publishDate 2020
physical 1 electronic resource (224 p.)
isbn 3-03943-118-8
3-03943-119-6
illustrated Not Illustrated
work_keys_str_mv AT knolkerhansjoachim recentadvancesinironcatalysis
status_str n
ids_txt_mv (CKB)5400000000044046
(oapen)https://directory.doabooks.org/handle/20.500.12854/69132
(EXLCZ)995400000000044046
carrierType_str_mv cr
is_hierarchy_title Recent Advances in Iron Catalysis
author2_original_writing_str_mv noLinkedField
_version_ 1787548734692786176
fullrecord <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>04159nam-a2201021z--4500</leader><controlfield tag="001">993546078104498</controlfield><controlfield tag="005">20231214133158.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr|mn|---annan</controlfield><controlfield tag="008">202105s2020 xx |||||o ||| 0|eng d</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(CKB)5400000000044046</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(oapen)https://directory.doabooks.org/handle/20.500.12854/69132</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(EXLCZ)995400000000044046</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Knölker, Hans-Joachim</subfield><subfield code="4">edt</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Recent Advances in Iron Catalysis</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Basel, Switzerland</subfield><subfield code="b">MDPI - Multidisciplinary Digital Publishing Institute</subfield><subfield code="c">2020</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 electronic resource (224 p.)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="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.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">English</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Research &amp; information: general</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">iron</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cross-coupling</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">aryl esters</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">C–O activation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Fe-catalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Kumada cross-coupling</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">iron complexes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">hydrogen transfer</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">reductive amination</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">alcohols</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">amines</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">decarbonylation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">alkylation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">spirocyclization</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">aldehyde</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cinnamamide</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">iron catalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">bis-(aryl)manganese</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">alkenyl halides</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">ate iron(II) complex</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">asymmetric catalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">nitrogen ligand</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">oxidative coupling</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">BINOL synthesis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">carbene</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">diazoalkane</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">C-H functionalization</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">catalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">borylation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Iron</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">C-H functionalisation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">pinacolborane</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">photochemistry</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">amidation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">iron(III) chloride</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">amides</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">esters</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">solvent-free</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">iron-catalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">carboazidation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">β-methyl scission</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">radical</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">DFT</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">organic synthesis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">C-H activation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">C-C coupling</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">α-alkenylation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">dehydrogenative coupling</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">sustainability</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">naphthidines</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">fluorescence</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">iron catalyst</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">ATRP</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">controlled radical polymerization</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">external stimuli</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">asymmetric transfer hydrogenation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">density functional theory</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">bifunctional catalyst</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">haloalkane coupling</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Grignard reagent</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">FeI/FeII/FeIII mechanism</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">3-03943-118-8</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">3-03943-119-6</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Knölker, Hans-Joachim</subfield><subfield code="4">oth</subfield></datafield><datafield tag="906" ind1=" " ind2=" "><subfield code="a">BOOK</subfield></datafield><datafield tag="ADM" ind1=" " ind2=" "><subfield code="b">2023-12-15 05:45:45 Europe/Vienna</subfield><subfield code="f">system</subfield><subfield code="c">marc21</subfield><subfield code="a">2022-04-04 09:22:53 Europe/Vienna</subfield><subfield code="g">false</subfield></datafield><datafield tag="AVE" ind1=" " ind2=" "><subfield code="i">DOAB Directory of Open Access Books</subfield><subfield code="P">DOAB Directory of Open Access Books</subfield><subfield code="x">https://eu02.alma.exlibrisgroup.com/view/uresolver/43ACC_OEAW/openurl?u.ignore_date_coverage=true&amp;portfolio_pid=5338136020004498&amp;Force_direct=true</subfield><subfield code="Z">5338136020004498</subfield><subfield code="b">Available</subfield><subfield code="8">5338136020004498</subfield></datafield></record></collection>