Highly efficient biocatalytic resolution of cis- and trans-3-aminoindan-1- ol: Syntheses of enantiopure orthogonally protected cis- and trans-indane-1,3-diamine

Chemistry - A European Journal

Volumn 10, Issue 12, 2004, Pages 3006-3014

  López García, Mónica ^a   Alfonso, Ignacio ^a   Gotor, Vicente ^a  

^a UNIVERSITY OF OVIEDO   (Spain)

Author keywords

Biotransformations; Chemoenzymatic synthesis; Enzymes; Mitsunobu reaction

Indexed keywords

ACETYLATION; ALCOHOLS; CATALYSIS; ISOMERS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

BIOCATALYSIS; REACTION CONDITIONS;

AMINES;

3 AMINOINDAN 1 OL; AMINE; AMINOALCOHOL; ENZYME; INDAN DERIVATIVE; INDANE 1,3 DIAMINE; LIPASE B; NITROGEN; UNCLASSIFIED DRUG;

ACETYLATION; ARTICLE; BIOCATALYST; CANDIDA ANTARCTICA; CIS ISOMER; DEPROTECTION REACTION; DIASTEREOISOMER; ENANTIOMER; ENANTIOSELECTIVITY; ENZYME MECHANISM; MITSUNOBU REACTION; MOLECULAR MODEL; NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; TRANS ISOMER;

AMINO ALCOHOLS; DIAMINES; INDANS; LIPASE; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; STEREOISOMERISM;

EID: 3042701337     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200306070     Document Type: Article

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