Substituent effect on exo stereoselectivity in the 1,3-dipolar cycloaddition reaction of tulipalin A with nitrile ylides

Journal of Organic Chemistry

Volumn 73, Issue 8, 2008, Pages 3032-3039

  Melša, Petr ^a   Čajan, Michal ^b   Havlas, Zdeněk ^c   Mazal, Ctibor ^a  

^a MASARYK UNIVERSITY   (Czech Republic)

^b PALACKÝ UNIVERSITY   (Czech Republic)

^c INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

1,3-DIPOLAR REAGENT; BENZYLIDE PHENYL RING; EXO-TRANSITION;

ACTIVATION ENERGY; AROMATIC COMPOUNDS; CYCLOADDITION; DENSITY FUNCTIONAL THEORY; STEREOSELECTIVITY;

SUBSTITUTION REACTIONS;

ALPHA METHYLENE BUTYROLACTONE; AMPHOLYTE; BENZENE DERIVATIVE; BENZONITRILE; CARBONYL DERIVATIVE; FURANONE DERIVATIVE; LACTONE DERIVATIVE; NITRILE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CORRELATION ANALYSIS; CYCLOADDITION; DENSITY FUNCTIONAL THEORY; DIASTEREOISOMER; ELECTRON TRANSPORT; ENERGY; MOLECULAR INTERACTION; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 42149156728     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702563n     Document Type: Article

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