Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles
This book is focused on metal-catalyzed cyclocarbonylation reactions applied to the synthesis of heterocyclic rings of different sizes, including diastereoselective and enantioselective approaches, homogeneous and heterogeneous metal catalysis, and the application of these reactions to the total syn...
Saved in:
Sonstige: | |
---|---|
Year of Publication: | 2022 |
Language: | English |
Physical Description: | 1 electronic resource (124 p.) |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
993545183004498 |
---|---|
ctrlnum |
(CKB)5680000000037733 (oapen)https://directory.doabooks.org/handle/20.500.12854/80950 (EXLCZ)995680000000037733 |
collection |
bib_alma |
record_format |
marc |
spelling |
Aronica, Laura Antonella edt Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles Basel MDPI - Multidisciplinary Digital Publishing Institute 2022 1 electronic resource (124 p.) text txt rdacontent computer c rdamedia online resource cr rdacarrier This book is focused on metal-catalyzed cyclocarbonylation reactions applied to the synthesis of heterocyclic rings of different sizes, including diastereoselective and enantioselective approaches, homogeneous and heterogeneous metal catalysis, and the application of these reactions to the total synthesis of natural products. English Research & information: general bicssc Chemistry bicssc Organic chemistry bicssc Cr-phthalocyanine porous organic polymer Friedel-Crafts reaction heterogeneous catalysis carbonylation β-lactones catalyst recyclability silylformylation silylcarbocyclization alkynes N-heterocycles O-heterocycles radical carbonylation acyl radical visible light photocatalysis heterocycles metal-mediated reactions Pauson-Khand reaction cyclopentenones natural products total syntheses Jaspine B flow chemistry palladium catalysis cyclisation 3-0365-3774-0 3-0365-3773-2 Aronica, Laura Antonella oth |
language |
English |
format |
eBook |
author2 |
Aronica, Laura Antonella |
author_facet |
Aronica, Laura Antonella |
author2_variant |
l a a la laa |
author2_role |
Sonstige |
title |
Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles |
spellingShingle |
Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles |
title_full |
Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles |
title_fullStr |
Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles |
title_full_unstemmed |
Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles |
title_auth |
Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles |
title_new |
Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles |
title_sort |
metal promoted cyclocarbonylation reactions in the synthesis of heterocycles |
publisher |
MDPI - Multidisciplinary Digital Publishing Institute |
publishDate |
2022 |
physical |
1 electronic resource (124 p.) |
isbn |
3-0365-3774-0 3-0365-3773-2 |
illustrated |
Not Illustrated |
work_keys_str_mv |
AT aronicalauraantonella metalpromotedcyclocarbonylationreactionsinthesynthesisofheterocycles |
status_str |
n |
ids_txt_mv |
(CKB)5680000000037733 (oapen)https://directory.doabooks.org/handle/20.500.12854/80950 (EXLCZ)995680000000037733 |
carrierType_str_mv |
cr |
is_hierarchy_title |
Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles |
author2_original_writing_str_mv |
noLinkedField |
_version_ |
1787548866938142720 |
fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02190nam-a2200601z--4500</leader><controlfield tag="001">993545183004498</controlfield><controlfield tag="005">20231214133354.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr|mn|---annan</controlfield><controlfield tag="008">202205s2022 xx |||||o ||| 0|eng d</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(CKB)5680000000037733</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(oapen)https://directory.doabooks.org/handle/20.500.12854/80950</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(EXLCZ)995680000000037733</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Aronica, Laura Antonella</subfield><subfield code="4">edt</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Metal Promoted Cyclocarbonylation Reactions in the Synthesis of Heterocycles</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Basel</subfield><subfield code="b">MDPI - Multidisciplinary Digital Publishing Institute</subfield><subfield code="c">2022</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 electronic resource (124 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">This book is focused on metal-catalyzed cyclocarbonylation reactions applied to the synthesis of heterocyclic rings of different sizes, including diastereoselective and enantioselective approaches, homogeneous and heterogeneous metal catalysis, and the application of these reactions to the total synthesis of natural products.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">English</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Research & information: general</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Chemistry</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Organic chemistry</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Cr-phthalocyanine</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">porous organic polymer</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Friedel-Crafts reaction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">heterogeneous catalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">carbonylation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">β-lactones</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">catalyst recyclability</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">silylformylation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">silylcarbocyclization</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">alkynes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">N-heterocycles</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">O-heterocycles</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">radical carbonylation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">acyl radical</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">visible light photocatalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">heterocycles</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">metal-mediated reactions</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Pauson-Khand reaction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cyclopentenones</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">natural products total syntheses</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Jaspine B</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">flow chemistry</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">palladium catalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cyclisation</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">3-0365-3774-0</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">3-0365-3773-2</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Aronica, Laura Antonella</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 05:52:02 Europe/Vienna</subfield><subfield code="f">system</subfield><subfield code="c">marc21</subfield><subfield code="a">2022-05-14 21:41:54 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&portfolio_pid=5337837420004498&Force_direct=true</subfield><subfield code="Z">5337837420004498</subfield><subfield code="b">Available</subfield><subfield code="8">5337837420004498</subfield></datafield></record></collection> |