Chemoenzymatic asymmetric synthesis of optically active pentane-1,5-diamine fragments by means of lipase-catalyzed desymmetrization transformations

Journal of Organic Chemistry

Volumn 76, Issue 14, 2011, Pages 5709-5718

  Ríos Lombardía, Nicolás ^a   Busto, Eduardo ^a   Gotor Fernández, Vicente ^a   Gotor, Vicente ^a  

^a UNIVERSITY OF OVIEDO   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

1 ,4-DIOXANE; ACYL DONORS; ALKOXYCARBONYLATION; AMINO GROUP; ASYMMETRIC SYNTHESIS; DESYM-METRIZATION; ENANTIOMERIC EXCESS; ISOLATED YIELD; LIPASE-CATALYZED; MONOAMIDES; OPTICALLY ACTIVE; OPTIMAL CONDITIONS; PSEUDOMONAS CEPACIA LIPASE; REACTION PARAMETERS; STEREO-SELECTIVE;

ETHERS; PARAFFINS; PROPANE;

SYNTHESIS (CHEMICAL);

1,4 DIOXNE; AMINO ACID; BACTERIAL ENZYME; BURKHOLDERIA CEPACIA LIPASE; CARBONIC ACID; DIAMINE DERIVATIVE; DIOXANE DERIVATIVE; ENZYME; ESTER; METHOXYACETIC ACID; NITROGEN; ORGANIC SOLVENT; PENTANE 1,5 DIAMINE; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; BIOCATALYST; CARBONYLATION; ENANTIOMER; ENZYME SYNTHESIS; NONHUMAN; POLYAMINE SYNTHESIS; TEMPERATURE;

BIOCATALYSIS; BURKHOLDERIA CEPACIA; CADAVERINE; LIPASE; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 79960188774     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo2007972     Document Type: Article

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