Controlling stereoselectivity by enzymatic and chemical means to access enantiomerically pure (1S,3R)-1-benzyl-2,3-dimethyl-1,2,3,4- tetrahydroisoquinoline derivatives

Tetrahedron Asymmetry

Volumn 24, Issue 12, 2013, Pages 744-749

  Orden, Alejandro A ^a   Schrittwieser, Joerg H ^b   Resch, Verena ^b   Mutti, Francesco G ^b   Kroutil, Wolfgang ^b  

^a UNIVERSIDAD NACIONAL DE SAN LUIS   (Argentina)

^b UNIVERSITY OF GRAZ   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

(1,3) 1 BENZYL 2,3 DIMETHYL 1,2,3,4 TETRAHYDROISOQUINOLINE; AMINOTRANSFERASE; CHARCOAL; IMINE; ISOQUINOLINE DERIVATIVE; PALLADIUM; PROPANE; UNCLASSIFIED DRUG;

AMINATION; ARTICLE; BIOCATALYSIS; CHEMISTRY; DIASTEREOSELECTIVITY; DRUG SYNTHESIS; ENANTIOMER; HYDROGENATION; PRIORITY JOURNAL; STEREOCHEMISTRY; SUBSTITUTION REACTION;

EID: 84879422243     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2013.05.003     Document Type: Article

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