Method for the enantioselective reduction of 3,5-dioxocarboxylic acids, their salts and their esters
US6399339B1 · kind B1 · utility
Assignee
Inventors
Key dates
| Filing date | Jul 10, 2001 |
| Grant date | Jun 4, 2002 |
| Priority date | — |
| Expiry date | Jul 10, 2021 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC12P41/002
- WIPO fieldBiotechnology
- WIPO sectorChemistry
Abstract
The invention relates to a method for the enantioselective reduction of 3,5-dioxocarboxylic acid derivatives and their syntheses. According to the invention, compounds of formula (4) are reacted with an alcohol dehydrogenase which preferably stems from Lactobacillus brevis and which is recombinantly over-expressed in Escherichia coli, in the presence of NADPH. The keto group in position 5 is enantioselectively reduced during this reaction. The keto group in position 3 can also be specifically syn- or anti-reduced in a further step by means of chemical or enzymatic reactions.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.