Synthesis of 2-alkenyl-1-pyrrolin-1-oxides and polysubstituted nitrones

Synthesis

Volumn , Issue 9, 2003, Pages 1367-1372

  Sár, Cecília ^a   Jeko, József ^b   Hideg, Kálmán ^a  

^a UNIVERSITY OF PÉCS   (Hungary)

^b ICN Hungary   (Hungary)

Author keywords

Aldol reactions; Free radicals; Grignard reactions; Ring opening

Indexed keywords

AMINES; ESTERS; OXIDATION; SUBSTITUTION REACTIONS;

POLYSUBSTITUTED NITRONES;

SYNTHESIS (CHEMICAL);

2 HEPTA 1,3 DIENYL 2,5,5 TRIMETHYLPYRROLIDIN 1 YLOXYL; 2 HYDROXY 3 (2,5,5 TRIMETHYL 1 OXYLPYRROLIDIN 2 YL)PROPIONIC ACID METHYL ESTER; 2 HYDROXY 3 (2,5,5 TRIMETHYLPYRROLIDIN 2 YL)PROPIONIC ACID METHYL ESTER; 2 METHYL 2 (2 PYRIDIN 4 YLVINYL) 3,4 DIHYDRO 2H PYRROLE 1 OXIDE; 2 [2 (4 CHLOROPHENYL)VINYL] 2,2,5 TRIMETHYLPYRROLIDIN 1 YLOXYL; 2,2 DIMETHYL 5 (2 PYRIDIN 4 YLVINYL) 3,4 DIHYDRO 2H PYRROLE 1 OXIDE; 2,2 DIMETHYL 5 UNDEC 1 ENYL 3,4 DIHYDRO 2H PYRROLE 1 OXIDE; 2,2 DIMETHYL 5 [2 (3,4,5 TRIMETHOXYPHENYL)VINYL] 3,4 DIHYDRO 2H PYRROLE 1 OXIDE; 2,2 DIMETHYL 5 [2 (4 NITROPHENYL)VINYL] 3,4 DIHYDRO 2H PYRROLE 1 OXIDE; 2,2,5 TRIMETHYL 5 (2 PYRIDIN 4 YLVINYL)PYRROLIDIN 1 YLOXYL; 2,2,5 TRIMETHYL 5 (4 PHENYLBUTA 1,3 DIENYL)PYRROLIDIN 1 YLOXYL; 2,2,5 TRIMETHYL 5 [2 (3,4,5 TRIMETHOXYPHENYL)VINYL]PYRROLIDIN 1 YLOXYL; 3 METHYL 5 (2,2,5 TRIMETHYLPYRROLIDIN 2 YL 1 OXYL)PENTA 2,4 DIENOIC ACID ETHYL ESTER; 3 METHYL 5 (5,5 DIMETHYL 1 OXIDE 4,5 DIHYDRO 3H PYRROL 2 YL)PENTA 2,4 DIENOIC ACID ETHYL ESTER; 3A,6,6 TRIMETHYLHEXAHYDROPYRROLO[1,2 B]ISOXAZOLE 2 CARBOXYLIC ACID METHYL ESTER; 3A,6,6 TRIMETHYLHEXAHYDROPYRROLO[1,2 B]ISOXAZOLE 3 CARBOXYLIC ACID METHYL ESTER; 5 [2 (4 CHLOROPHENYL)VINYL] 2,2 DIMETHYL 3,4 DIHYDRO 2H PYRROLE 1 OXIDE; 5,5 DIMETHYL 1 PYRROLINE 1 OXIDE; ALDEHYDE; ALPHA HYDROXY NITROXIDE ESTER; AMINE; ESTER DERIVATIVE; IODINE; MAGNESIUM; NITRONE DERIVATIVE; NITROXIDE DERIVATIVE; OXIDE; PYRROLE DERIVATIVE; PYRROLIDINE DERIVATIVE; PYRROLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; METHYLATION; OXIDATION; SYNTHESIS;

EID: 18744425423     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-40207     Document Type: Article

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