Expanding the scope of Metal-Free enantioselective allylic substitutions: Anthrones
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F15%3A10314003" target="_blank" >RIV/00216208:11310/15:10314003 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1038/srep16886" target="_blank" >http://dx.doi.org/10.1038/srep16886</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/srep16886" target="_blank" >10.1038/srep16886</a>
Alternative languages
Result language
angličtina
Original language name
Expanding the scope of Metal-Free enantioselective allylic substitutions: Anthrones
Original language description
The highly enantioselective asymmetric allylic alkylation of Morita-Baylis-Hillman carbonates with anthrones is presented. The reaction is simply catalyzed by cinchona alkaloid derivatives affording the final alkylated products in good yields and excellent enantioselectivities.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—
Result continuities
Project
—
Continuities
S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2015
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Scientific Reports
ISSN
2045-2322
e-ISSN
—
Volume of the periodical
5
Issue of the periodical within the volume
November
Country of publishing house
GB - UNITED KINGDOM
Number of pages
9
Pages from-to
1-9
UT code for WoS article
000365238800003
EID of the result in the Scopus database
2-s2.0-84947939141