Oxahelicene NHC ligands in the asymmetric synthesis of nonracemic helicenes
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F17%3A00475336" target="_blank" >RIV/61388963:_____/17:00475336 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1039/c7cc00781g" target="_blank" >http://dx.doi.org/10.1039/c7cc00781g</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c7cc00781g" target="_blank" >10.1039/c7cc00781g</a>
Alternative languages
Result language
angličtina
Original language name
Oxahelicene NHC ligands in the asymmetric synthesis of nonracemic helicenes
Original language description
A straightforward approach to enantiopure 2H-pyran-modified amino-[5]helicenes and amino[6]helicenes was developed. They were converted to 1,3-disubstituted imidazolium salts and used as NHC ligand precursors in the Ni-0-catalysed enantioselective [2+2+2] cycloisomerisation of aromatic triynes to obtain the model helicene derivatives in up to 86% ee.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10401 - Organic chemistry
Result continuities
Project
<a href="/en/project/GA14-29667S" target="_blank" >GA14-29667S: The preparation of enantiopure helically chiral aromatics and their use in catalysis</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Chemical Communications
ISSN
1359-7345
e-ISSN
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Volume of the periodical
53
Issue of the periodical within the volume
31
Country of publishing house
GB - UNITED KINGDOM
Number of pages
4
Pages from-to
4370-4373
UT code for WoS article
000399729100019
EID of the result in the Scopus database
2-s2.0-85017558310