Producing enantiomerically enriched nitroalkane compounds, comprises reacting prochiral nitroalkene compounds in the presence of a biocatalyst in highly enantioselective manner

Publication: DE102012022670A1
Published: 2014-05-22
Family Size: 2
Granted: No

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

C12P13/00

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

For further information please contact the transfer office.