Highly Enantioselective Addition of 1-Fluoro-1-nitro(phenylsulfonyl)methane to alpha,beta-Unsaturated Aldehydes
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F10%3A10070155" target="_blank" >RIV/00216208:11310/10:10070155 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Highly Enantioselective Addition of 1-Fluoro-1-nitro(phenylsulfonyl)methane to alpha,beta-Unsaturated Aldehydes
Original language description
An organocatalytic, highly enantioselective addition of 1- fluoro-1-nitro(phenylsulfonyl)methane to alfa,beta-unsaturated aldehydes is reported. The reaction is simply catalyzed by secondary amines and furnishes the corresponding fluorinated derivativesin good yields, with moderate diastereoselectivities 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
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Result continuities
Project
<a href="/en/project/GP203%2F09%2FP193" target="_blank" >GP203/09/P193: Enantioselective synthesis of N- and S-containing heterocycles via organocatalysis: The way for preparation of biologically active compounds.</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2010
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
European Journal of Organic Chemistry
ISSN
1434-193X
e-ISSN
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Volume of the periodical
2010
Issue of the periodical within the volume
28
Country of publishing house
GB - UNITED KINGDOM
Number of pages
7
Pages from-to
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UT code for WoS article
000283387900017
EID of the result in the Scopus database
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