Process for the enantioselective preparation of (.beta.-1)-hydroxyalkylxanthines by reduction using Rhodotorula rubra
US5310666A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | Nov 13, 1992 |
| Grant date | May 10, 1994 |
| Priority date | — |
| Expiry date | Nov 13, 2012 |
Classification
- Technology area (CPC Y)Emerging Cross-Sectional Technologies
- CPC primaryY10S435/911
- WIPO fieldOrganic fine chemistry
- WIPO sectorChemistry
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.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.