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Highly enantioselective synthesis of chiral cyclic allylic amines via Rh-catalyzed asymmetric hydrogenation
- Source :
- Organic letters. 16(13)
- Publication Year :
- 2014
-
Abstract
- Highly regioselective and enantioselective asymmetric hydrogenation of cyclic dienamides catalyzed by an Rh-DuanPhos complex has been developed, which provides a readily accessible method for the synthesis of chiral cyclic allylic amines in excellent enantioselectivities (up to 99% ee). The products are valuable chiral building blocks and could be easily transformed to multisubstituted cyclohexane derivatives.
- Subjects :
- Allylic rearrangement
Cyclohexane
Molecular Structure
Chemistry
Organic Chemistry
Asymmetric hydrogenation
Enantioselective synthesis
Regioselectivity
Stereoisomerism
Biochemistry
Catalysis
chemistry.chemical_compound
Benzene Derivatives
Organic chemistry
Rhodium
Hydrogenation
Physical and Theoretical Chemistry
Amines
Subjects
Details
- ISSN :
- 15237052
- Volume :
- 16
- Issue :
- 13
- Database :
- OpenAIRE
- Journal :
- Organic letters
- Accession number :
- edsair.doi.dedup.....18d8b1d5ec8206c362ee42f1223b5aa4