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Short total synthesis of (-)-kainic acid
- Source :
- Organic letters. 16(9)
- Publication Year :
- 2014
-
Abstract
- A short total synthesis of (−)-kainic acid has been developed involving a novel diastereofacial differentiating Cu-catalyzed Michael addition–cyclization reaction, which provided access to a chiral pyrroline in a highly stereoselective manner. The chiral pyrroline was converted to (−)-kainic acid via the stereoselective 1,4-reduction of the pyrroline double bond in three steps.
- Subjects :
- chemistry.chemical_classification
Kainic acid
Kainic Acid
Double bond
Molecular Structure
Stereochemistry
Organic Chemistry
Total synthesis
Stereoisomerism
Pyrroline
Biochemistry
Catalysis
chemistry.chemical_compound
chemistry
Stereoselectivity
Pyrroles
Physical and Theoretical Chemistry
Oxidation-Reduction
Copper
Subjects
Details
- ISSN :
- 15237052
- Volume :
- 16
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- Organic letters
- Accession number :
- edsair.doi.dedup.....add02d981d0930e2f7bfb7ba511aefc6