Synthesis of optically active γ-lactones via lipase-catalyzed resolution

Flavour and Fragrance Journal

Volumn 22, Issue 5, 2007, Pages 421-429

  Shimotori, Yasutaka ^a   Nakahachi, Yukihiko ^a   Inoue, Keita ^a   Miyakoshi, Tetsuo ^a  

^a MEIJI UNIVERSITY   (Japan)

Author keywords

lactone; Kinetic resolution; N methyl 4 acetoxyalkanamide; N methyl 4 hydroxyalkanamide; Novozym 435

Indexed keywords

ACETYLATION; CATALYSIS; ENANTIOSELECTIVITY; ESTERS; HYDROLYSIS; LIPASES; SYNTHESIS (CHEMICAL);

ENANTIOSELECTIVE ACETYLATION; GRIGNARD REACTION; KINETIC RESOLUTION; LACTONES;

ENANTIOMERS;

AMIDE; GAMMA LACTONE DERIVATIVE; SUCCINIC ANHYDRIDE; TRIACYLGLYCEROL LIPASE;

ACETYLATION; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CONTROLLED STUDY; ENANTIOMER; ENANTIOSELECTIVITY; GRIGNARD REACTION; HYDROLYSIS; MELTING POINT; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; RING OPENING; SYNTHESIS; THIN LAYER CHROMATOGRAPHY;

EID: 34548679606     PISSN: 08825734     EISSN: 10991026     Source Type: Journal    
DOI: 10.1002/ffj.1816     Document Type: Article

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