Quantifying asymmetry in concerted reactions: Solvents effect on a diels-alder cycloaddition

Journal of Organic Chemistry

Volumn 76, Issue 12, 2011, Pages 4973-4979

  Tuvi Arad, Inbal ^a   Avnir, David ^b  

^a OPEN UNIVERSITY OF ISRAEL   (Israel)

^b HEBREW UNIVERSITY OF JERUSALEM   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ASYNCHRONICITY; CHARGE SEPARATIONS; CONCERTED REACTIONS; CONTINUOUS SYMMETRY; DIELS-ALDER CYCLOADDITIONS; ENTHALPY OF ACTIVATION; GEOMETRICAL PARAMETERS; MINIMAL VALUE; MINIMUM ENERGY PATHS; PREDICTIVE VALUES; QUANTITATIVE TREATMENT; STRUCTURAL PARAMETER; TETRACYANOETHYLENE; TRANSITION STATE;

BUTADIENE; ENTHALPY; SOLVENTS; TEACHING;

CYCLOADDITION;

1,3 BUTADIENE DERIVATIVE; 1,4 DIMETHOXY 1,3 BUTADIENE; SOLVENT; TETRACYANOETHYLENE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CYCLOADDITION; DIELS ALDER REACTION; ENTHALPY; GEOMETRY; ORGANIC CHEMISTRY; REACTION ANALYSIS;

EID: 79958854383     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo200648h     Document Type: Article

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