A study towards efficient L-threonine aldolase-catalyzed enantio- and diastereoselective aldol reactions of glycine with substituted benzaldehydes: Biocatalyst production and process development

Tetrahedron Asymmetry

Volumn 22, Issue 9, 2011, Pages 925-928

  Baer, Katrin ^a   Dückers, Nina ^b   Rosenbaum, Thorsten ^c   Leggewie, Christian ^b   Simon, Sabine ^a   Kraußer, Marina ^a   Oßwald, Steffen ^d   Hummel, Werner ^c,e   Gröger, Harald ^a,e  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^b Evocatal GmbH   (Germany)

^c HEINRICH HEINE UNIVERSITY   (Germany)

^d EVONIK DEGUSSA GMBH   (Germany)

^e BIELEFELD UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

2 CHLOROBENZALDEHYDE; AMINO ACID DERIVATIVE; BENZALDEHYDE DERIVATIVE; BETA HYDROXY ALPHA AMINO ACID; GLYCINE; THREONINE ALDOLASE; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; BIOCATALYST; BIOTRANSFORMATION; ENANTIOMER; ENANTIOSELECTIVITY; ESCHERICHIA COLI; FERMENTATION; NONHUMAN; PRIORITY JOURNAL; PROCESS DEVELOPMENT; SACCHAROMYCES CEREVISIAE;

EID: 79960953596     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2011.04.016     Document Type: Article

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