Enantioselective Organocatalytic Amination of Pyrazolones
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F13%3A10159268" target="_blank" >RIV/00216208:11310/13:10159268 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1002/ajoc.201200168" target="_blank" >http://dx.doi.org/10.1002/ajoc.201200168</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/ajoc.201200168" target="_blank" >10.1002/ajoc.201200168</a>
Alternative languages
Result language
angličtina
Original language name
Enantioselective Organocatalytic Amination of Pyrazolones
Original language description
The organocatalytic enantioselective amination of pyrazolones is reported. The reaction between pyrazolones and diazodicarboxylates is simple and is catalyzed by quinine to afford the final aminopyarazolone derivatives in excellent yields and good enantioselectivity.
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
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Result continuities
Project
<a href="/en/project/GAP207%2F10%2F0428" target="_blank" >GAP207/10/0428: Enantioselective organocatalytic alpha-alkynylation,alkenylation and arylation of aldehydes and ketones</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
ASIAN JOURNAL OF ORGANIC CHEMISTRY
ISSN
2193-5807
e-ISSN
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Volume of the periodical
2
Issue of the periodical within the volume
1
Country of publishing house
DE - GERMANY
Number of pages
5
Pages from-to
64-68
UT code for WoS article
000325949000006
EID of the result in the Scopus database
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