Enzymatic preparation of chiral 1-phenylglycidols and 1-phenyl-1,2-propanediols

Tetrahedron: Asymmetry

Volumn 3, Issue 11, 1992, Pages 1369-1372

  Takeshita, Mitsuhiro ^a   Yaguchi, Reiko ^a   Akutsu, Nami ^a  

^a TOHOKU PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1 PHENYL 1,2 PROPANEDIOL; ALKANOL; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

ARTICLE; ENZYME ACTIVITY; REACTION ANALYSIS; SYNTHESIS; YEAST;

EID: 0026437377     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/0957-4166(92)80008-K     Document Type: Article

References (23)

1. General Aspects and Optimization of Enantioselective Biocatalysis in Organic Solvents: The Use of Lipases[New Synthetic Methods(76)]
2. Highly efficient lipase-catalyzed asymmetric synthesis of chiral glycerol derivatives leading to practical synthesis of s-propranolol
3. Synthesis of optically active 1-phenyl-1,2-propanediol by use of baker's yeast.
4. Reductive C2-homologation of substituted benzaldehydes by fermenting baker's yeast.
5. Highly diastereocontrolled reduction of ketones by means of hydrosilanes. Practical synthesis of optically active 1,2-diols and 2-amino alcohols of threo or erythro configuration
6. Synthesis of optically active 1-phenyl-1,2-propanediol by use of baker's yeast.
7. Regioselective titanium mediated reductive opening of 2,3-epoxy alcohols