Producing enantiomerically enriched nitroalkane compounds, comprises reacting prochiral nitroalkene compounds in the presence of a biocatalyst in highly enantioselective manner
Simple SummaryContent extracted from patent full text and abstract with AI.
This patent describes a method to produce enantiomerically enriched (chiral) nitroalkane compounds by reacting prochiral nitroalkene compounds with a biocatalyst. The process is highly selective and results in products with an enantiomeric excess greater than 90%.
Use CasesContent extracted from patent full text and abstract with AI.
- Manufacturing of chiral intermediates for pharmaceutical synthesis
- Production of agrochemicals where chirality is essential for activity or safety
- Creation of fine chemicals for use in fragrances or flavors requiring specific enantiomers
- Research in organic and medicinal chemistry requiring pure enantiomers
BenefitsContent extracted from patent full text and abstract with AI.
- Achieves high enantiomeric purity (over 90%) in the target compounds
- Utilizes biocatalysts, which are safer and greener compared to traditional chemical catalysts
- Enables the efficient and scalable synthesis of valuable chiral building blocks
- Potentially reduces production costs by simplifying chiral separation processes
Technical Classifications (CPCs)
Main Classifications
Chemistry & Materials Science
Sub Classifications
Biochemistry, Beer & Spirits
CPC Codes
Inventors & Applicants
Applicants
Friedrich Alexander Universität Erlangen Nürnberg
Universität Bielefeld
Patent Abstract
Producing enantiomerically enriched nitroalkane compounds (I) or (II), comprises reacting prochiral nitroalkene compounds (III) in the presence of a biocatalyst in highly enantioselective manner, where enantiomeric excesses of desired product of (I) or (II) are greater than 90%. Producing enantiomerically enriched nitroalkane compounds of formula (I) or (II), comprises reacting prochiral nitroalkene compounds of formula (III) in the presence of a biocatalyst in highly enantioselective manner, where enantiomeric excesses of desired product of (I) or (II) are greater than 90%. Ar1 : aryl; and R : CH 3, CH 2OH. [Image].
Key Information
Publication No.
DE102012022670A1
Family ID
50625337
Publication Date
2014-05-22
Application No.
DE102012022670A
Application Date
2012-11-21
Priority Date
2012-11-21
Granted
No
Possible Cooperation
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