Process for the enantioselective preparation of (.beta.-1)-hydro

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing heterocyclic carbon compound having only o – n – s,...

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435280, 435822, C12P 1718

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active

053106660

ABSTRACT:
A Rhodotorula rubra strain has been found which reduces pentoxifylline to 100% to give the S-alcohol. Moreover, other oxoalkylxanthine derivatives can also be converted into the corresponding S-alcohol. The microbiologically obtained S-(+)-enantiomers can then be converted stereoselectively into the respective R-(-)-enantiomers. The corresponding S-alcohols and the R-alcohols obtained by enantioselective inversion of configuration cause an increase in cerebral blood flow.

REFERENCES:
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Smith et al., J. Chrom. 281: 281-287 (1983).
Davis et al., Appl. Env. Microbiology 48: 327-331 (1984).
Jones et al., Tetrahedron 42: 3351-3403 (1986).
Davis et al, Xenobiotica 12: 1001-1010 (1985).
Mitteilung, European Search Report, dated Jun. 17, 1992.

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