Action of L-aminoacylase and L-amino acid oxidase on 2-amino-3- methylpent-4-enoic acid [Δ(4)-dehydroisoleucine and alloisoleucine] stereoisomers: An alternative route to a stereochemically pure compound and the application to the synthesis of (R)-2-methylbutan-1-ol

Synthesis

Volumn , Issue 9, 1999, Pages 1671-1677

  Bakke, Mikio ^a   Ohta, Hiromichi ^a   Kazmaier, Uli ^b   Sugai, Takeshi ^a  

^a KEIO UNIVERSITY   (Japan)

^b UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

(R) 2 methylbutan 1 ol; Chelation controlled enolate Claisen rearrangement; L alloisoleucine; L amino acids oxidase; L aminoacylase

Indexed keywords

ALLOISOLEUCINE; AMINO ACID DERIVATIVE; BUTANOL;

ARTICLE; CHELATION; CHEMICAL REACTION; HYDROLYSIS; STEREOCHEMISTRY; STEREOISOMERISM; SYNTHESIS;

EID: 0032882133     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-3565     Document Type: Article

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