Novel protocol for the asymmetric synthesis of 3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one via bakers' yeast reduction

Heterocycles

Volumn 66, Issue 1, 2005, Pages 147-151

  Komiyama, Takuzo ^a   Takaguchi, Yutaka ^a   Tsuboi, Sadao ^a  

^a OKAYAMA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33646875725     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-05-S(K)57     Document Type: Article

References (18)

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16. 4 and evaporated. The residual crude products were purified by column-chromatography (hexane: EtOAc=15: 1) to give β-arylthio-α-hydroxy ester (2e) (17 mg, 28%).
17. 6S: C, 59.24; H, 5.72; N, 3.45. Found: C, 59.39; H, 5.66; N, 3.72.
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