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Volumn 74, Issue 6, 2009, Pages 2328-2336
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Understanding the stereoselection induced by chiral anthracene templates in diels-alder cycloaddition: A DFT study
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Author keywords
[No Author keywords available]
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Indexed keywords
ANTIPERIPLANAR;
BIOLOGICALLY ACTIVE MOLECULES;
BOLTZMANN DISTRIBUTIONS;
BUTENOLIDES;
CARBONYL OXYGENS;
DENSITY FUNCTIONAL THEORY METHODS;
DFT STUDIES;
DIASTEREO SELECTIVITIES;
DIASTEREOMER;
DIASTEREOMERIC;
DIASTEREOMERS;
DIASTEREOSELECTIVE;
DIELS-ALDER CYCLOADDITION;
DIENOPHILE;
FAVORABLE INTERACTIONS;
KEY ELEMENTS;
LONE PAIRS;
METHOXY;
OUT OF PLANES;
PRODUCT DISTRIBUTIONS;
REACTION CENTERS;
RELATED COMPOUNDS;
SMALL ENERGIES;
STEREOCENTER;
TRANSITION STATE;
AMIDES;
AMINES;
ANTHRACENE;
BOLTZMANN EQUATION;
HYDROGEN;
MALEIC ANHYDRIDE;
OXYGEN;
PROBABILITY DENSITY FUNCTION;
RELIABILITY THEORY;
STEREOCHEMISTRY;
UNSATURATED COMPOUNDS;
DENSITY FUNCTIONAL THEORY;
9 (1 METHOXY 2,2,2 TRIFLUOROETHYL)ANTHRACENE;
9 (1 METHOXYETHYL)ANTHRACENE;
9 (1 PHENYLETHYL)AMINOANTHRACENE;
ANTHRACENE;
BUTENOLIDE;
LACTAM DERIVATIVE;
MALEIC ANHYDRIDE;
NITROGEN;
OXYGEN;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CHIRALITY;
CYCLOADDITION;
DENSITY FUNCTIONAL THEORY;
DIASTEREOISOMER;
DIELS ALDER REACTION;
ENANTIOMER;
REACTION ANALYSIS;
RELIABILITY;
STEREOCHEMISTRY;
ANTHRACENES;
CONSERVATION OF NATURAL RESOURCES;
MALEIC ANHYDRIDES;
ORGANIC CHEMISTRY PROCESSES;
STEREOISOMERISM;
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EID: 64149129358
PISSN: 00223263
EISSN: None
Source Type: Journal
DOI: 10.1021/jo802365v Document Type: Article |
Times cited : (12)
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References (30)
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