A new synthetic route to highly enantioenriched 3-substituted-2,3-dihydro-1H-isoindol-1-ones

Tetrahedron Asymmetry

Volumn 14, Issue 15, 2003, Pages 2253-2258

  Deniau, Eric ^a   Enders, Dieter ^b   Couture, Axel ^a   Grandclaudon, Pierre ^a  

^a UNITÉ DE CATALYSE ET DE CHIMIE DU SOLIDE   (France)

^b RWTH AACHEN UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

2 (2 METHOXYMETHYLPYRROLIDIN 1 YL) (3 PHENYL 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 2 (2 METHOXYMETHYLPYRROLIDIN 1 YL) 3 (2 METHOXYPHENYL) 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 2 (2 METHOXYMETHYLPYRROLIDIN 1 YL) 3 (3 METHOXYPHENYL) 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 2 (2 METHOXYMETHYLPYRROLIDIN 1 YL) 3 (NAPHTHALEN 2 YL) 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 2 (2 METHOXYMETHYLPYRROLIDIN 1 YL) 3 METHYL 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 3 (2 METHOXYPHENYL) 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 3 (3 METHOXYPHENYL) 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 3 (NAPHTHALEN 2 YL) 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 3 METHYL 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 3 PHENYL 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 3 TERT BUTYL 2 (2 METHOXYMETHYLPYRROLIDIN 1 YL) 2,3 DIHYDRO 1H ISOINDOL 1 ONE; 3 TERT BUTYL 2,3 DIHYDRO 1H ISOINDOL 1 ONE; ISOINDOLE DERIVATIVE; UNCLASSIFIED DRUG;

ACIDITY; ARTICLE; ENANTIOMER; PRIORITY JOURNAL; REDUCTION; STEREOCHEMISTRY; SUBSTITUTION REACTION; SYNTHESIS;

EID: 0041402770     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(03)00409-9     Document Type: Article

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