Show simple item record
dc.contributor.author |
Bartáček, Jan
|
|
dc.contributor.author |
Svoboda, Jan
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dc.contributor.author |
Kocúrik, Martin
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dc.contributor.author |
Pochobradský, Jaroslav
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dc.contributor.author |
Čegan, Alexander
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dc.contributor.author |
Sedlák, Miloš
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dc.contributor.author |
Váňa, Jiří
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dc.date.accessioned |
2022-06-03T12:25:11Z |
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dc.date.available |
2022-06-03T12:25:11Z |
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dc.date.issued |
2021 |
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dc.identifier.issn |
1860-5397 |
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dc.identifier.uri |
https://hdl.handle.net/10195/79244 |
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dc.description.abstract |
The transition metal (palladium)-catalysed asymmetric 1,4-addition of arylboronic acids to conjugated enones belong to the most important and emerging strategies for the construction of C-C bonds in an asymmetric fashion. This review covers known catalytic systems used for this transformation. For clarity, we are using the type of ligand as a sorting criterion. Finally, we attempted to create a flowchart facilitating the selection of a suitable ligand for a given combination of enone and arylboronic acid. |
eng |
dc.format |
p. 1048-1085 |
eng |
dc.language.iso |
eng |
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dc.publisher |
Beilstein-Institut |
eng |
dc.relation.ispartof |
Beilstein Journal of Organic Chemistry, volume 17, issue: 1 |
eng |
dc.rights |
open access |
eng |
dc.rights.uri |
https://creativecommons.org/licenses/by/4.0/ |
|
dc.subject |
asymmetric reaction |
eng |
dc.subject |
arylboronic acids |
eng |
dc.subject |
conjugated enones |
eng |
dc.subject |
chromones |
eng |
dc.subject |
enantioselective catalysis |
eng |
dc.subject |
Michael addition |
eng |
dc.subject |
Pd complexes |
eng |
dc.subject |
asymetrická reakce |
cze |
dc.subject |
arylboronové kyseliny |
cze |
dc.subject |
konjugované enony |
cze |
dc.subject |
chromony |
cze |
dc.subject |
enantioselektivní katalýza |
cze |
dc.subject |
Michaelova adice |
cze |
dc.subject |
Pd komplexy |
cze |
dc.title |
Recent advances in palladium-catalysed asymmetric 1,4-additions of arylboronic acids to conjugated enones and chromones |
eng |
dc.title.alternative |
Pokroky v palladiem katalyzované asymetrické 1,4-adici arylboronových kyselin na konjugované enony a chromony |
cze |
dc.type |
article |
eng |
dc.description.abstract-translated |
Asymetrická 1,4-adice arylboronových kyselin na konjugované enony katalyzovaná přechodným kovem (palladiem) patří k nejdůležitějším a novým strategiím pro konstrukci C–C vazeb asymetrickým způsobem. Toto review zahrnuje známé katalytické systémy, které jsou pro tyto transformace využívány. Jako řadící kritérium jsme zvolili typ ligandu. Nakonec jsme vytvořili vývojový diagram, který má usnadnit výběr vhodného ligandu pro danou kombinaci enonu a arylboronové kyseliny. |
cze |
dc.peerreviewed |
yes |
eng |
dc.publicationstatus |
published version |
eng |
dc.identifier.doi |
10.3762/bjoc.17.84 |
|
dc.relation.publisherversion |
https://www.beilstein-journals.org/bjoc/articles/17/84 |
|
dc.project.ID |
SGS_2021_004/Nové organické sloučeniny a materiály ? jejich syntéza, charakterizace, reaktivita, užitné vlastnosti a bezpečnostní aspekty při zacházení s nimi. |
cze |
dc.identifier.wos |
000651413000001 |
|
dc.identifier.scopus |
2-s2.0-85105658569 |
|
dc.rights.license |
CC BY 4.0 |
|
dc.identifier.obd |
39886090 |
|
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