An effective approach to the enantiomers of alicyclic β-aminonitriles by using lipase catalysis

Tetrahedron Asymmetry

Volumn 16, Issue 22, 2005, Pages 3690-3697

  Fitz, Mónika ^a,b   Lundell, Katri ^a   Lindroos, Maria ^a   Fülöp, Ferenc ^b   Kanerva, Liisa T ^a  

^a UNIVERSITY OF TURKU   (Finland)

^b UNIVERSITY OF SZEGED   (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINOCYCLOHEXANECARBONITRILE; 2 AMINOCYCLOPENTANECARBONITRILE; 2 TERT BUTOXYCARBONYLAMINOCYCLOHEXANECARBONITRILE; 2 TERT BUTOXYCARBONYLAMINOCYCLOHEXANECARBOXAMIDE; 2,2,2 TRIFLUOROETHYL BUTANOATE; 7 TERT BUTOXYCARBONYL 7 AZABICYCLO[4.2.0]HEXAN 8 ONE; ALICYCLIC COMPOUND; BUTYRIC ACID; CYANIDE; TERT BUTYL METHYL ETHER; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; BURKHOLDERIA CEPACIA; CANDIDA ANTARCTICA; CATALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; ENANTIOSELECTIVITY; PRIORITY JOURNAL; RACEMIZATION; ROOM TEMPERATURE;

EID: 27944442041     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2005.10.017     Document Type: Article

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