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Volumn 10, Issue 14, 2012, Pages 2840-2846
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Highly efficient asymmetric Michael addition of aldehyde to nitroolefin using perhydroindolic acid as a chiral organocatalyst
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Author keywords
[No Author keywords available]
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Indexed keywords
BICYCLIC STRUCTURE;
C ATOMS;
CATALYST LOADINGS;
CATALYTIC EFFICIENCIES;
CHEMICAL YIELDS;
DIASTEREO- AND ENANTIOSELECTIVITY;
INDUSTRIAL PRODUCTION;
MICHAEL ADDITION REACTIONS;
MICHAEL ADDITIONS;
NITROOLEFINS;
OPTIMAL CONDITIONS;
ORGANOCATALYSTS;
TRANDOLAPRIL;
ADDITION REACTIONS;
ALDEHYDES;
AMINO ACIDS;
CATALYSTS;
LOADING;
ORGANIC COMPOUNDS;
ALDEHYDE;
ALKENE;
HETEROCYCLIC CARBOXYLIC ACID;
NITROGEN DERIVATIVE;
ARTICLE;
CATALYSIS;
CHEMICAL STRUCTURE;
CHEMISTRY;
STEREOISOMERISM;
SYNTHESIS;
ACIDS, HETEROCYCLIC;
ALDEHYDES;
ALKENES;
CATALYSIS;
MOLECULAR STRUCTURE;
NITROGEN COMPOUNDS;
STEREOISOMERISM;
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EID: 84864384992
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/c2ob00003b Document Type: Article |
Times cited : (26)
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References (50)
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