First Enantioselective Organocatalytic Addition of Nitromethylphenylsulfone to Enals. Enantioselective Synthesis of Cyclohexenones Bearing 3 Contiguousstereogeniccenters

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F13%3A10159145" target="_blank" >RIV/00216208:11310/13:10159145 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.2174/1570179411310030008" target="_blank" >http://dx.doi.org/10.2174/1570179411310030008</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.2174/1570179411310030008" target="_blank" >10.2174/1570179411310030008</a>

Result language
angličtina
Original language name
First Enantioselective Organocatalytic Addition of Nitromethylphenylsulfone to Enals. Enantioselective Synthesis of Cyclohexenones Bearing 3 Contiguousstereogeniccenters
Original language description
A highly enantioselectiveorganocatalyticnitromethylphenylsulfone addition to aliphatic alpha, beta-unsaturated aldehydes is reported. The reaction is catalyzed by simple and commercially available secondary amines, affording the cyclic compounds in moderate yields, good diastereoselectivities and excellent enantioselectivities.
Czech name
—
Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—

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

Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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