Indexed keywords
CATALYSIS;
FREE RADICALS;
HEAT TREATMENT;
MICROWAVES;
MOLECULAR DYNAMICS;
TIN;
ALLYLATIONS;
NITROXIDES;
PD CATALYSIS;
RADICAL CHEMISTRY;
PALLADIUM;
AMINE;
CARBOXYLIC ACID DERIVATIVE;
DIMETHYL 2 [2 PHENYLVINYL]CYCLOPENTANE 4 (2,2,6,6 TETRAETHYL 4 HYDROXYPIPERIDIN 1 YLOXY) 1,1 DICARBOXYLATE;
DIMETHYL 2 [3 METHYLBUT 1 ENYL]CYCLOHEXANE 5 (2,2,6,6 TETRAETHYL 4 HYDROXYPIPERIDIN 1 YLOXY) 1 1 DICARBOXYLATE;
DIMETHYL 2 [3 METHYLBUT 1 ENYL]CYCLOPENTANE 4 (2,2,6,6 TETRAETHYL 4 HYDROXYPIPERIDIN 1 YLOXY) 1,1 DICARBOXYLATE;
DIMETHYL 2 [PROP 1 ENYL]CYCLOPENTANE 4 (2,2,6,6 TETRAETHYL 4 HYDROXYPIPERIDIN 1 YLOXY) 1,1 DICARBOXYLATE;
ETHYL 1 (2,2 DIMETHYLPROPANOYL) 2 [2 PHENYLVINYL]CYCLOPENTANE 4 (2,2,6,6 TETRAETHYL 4 HYDROXYPIPERIDIN 1 YLOXY)CARBOXYLATE;
ETHYL 1 (2,2 DIMETHYLPROPANOYL) 2 [3 METHYLBUT 1 ENYL]CYCLOPENTANE 4 (2,2,6,6 TETRAETHYL 4 HYDROXYPIPERIDIN 1 YLOXY)CARBOXYLATE;
ETHYL 1 (2,2 DIMETHYLPROPANOYL)2 [PROP 1 ENYL]CYCLOPENTANE 4 (2,2,6,6 TETRAETHYL 4 HYDROXYPIPERIDIN 1 YLOXY)CARBOXYLATE;
UNCLASSIFIED DRUG;
ACYLATION;
ALLYLATION;
ARTICLE;
CATALYSIS;
CHEMICAL STRUCTURE;
CYCLIZATION;
HORNER WADSWORTH EMMONS REACTION;
ISOMERIZATION;
MICROWAVE IRRADIATION;
RADICAL REACTION;
REFORMATSKY REACTION;
2
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note
Diene 1d turned out to be unstable under the reaction conditions.
34
33746064553
note
Compounds 5a-d were isolated as 1:1 mixture of diastereoisomers. The isomers could not be separated. For 6a-c all four isomers (ratio 1:1:1:1) were formed. These isomers could not be separated.
36
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33746037276
note
The isomers could not be separated. Due to the complexity of the NMR spectra, the determination of the diastereoisomeric ratio for compounds 9a and 9c was not possible. For 9b the product was formed as a 30:12:3:1 mixture of isomers.
38
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