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Enantioselective Dearomatization of Alkylpyridiniums by N-Heterocyclic Carbene-Catalyzed Nucleophilic Acylation
- Source :
- The Journal of Organic Chemistry. 83:2050-2057
- Publication Year :
- 2018
- Publisher :
- American Chemical Society (ACS), 2018.
-
Abstract
- A chiral NHC-catalyzed dearomatizing reaction of activated N-alkylpyridinium salts with aliphatic aldehydes is described. The resulting acylated 1,4-dihydropyridines have been obtained with complete C4 regioselectivity and enantioselectivities in the range 52-78% ee. The (4R)-absolute configuration of the synthesized compounds has been determined by the TD-DFT simulation of the electronic circular dichroism spectra.
- Subjects :
- Organic Chemistry, N-heterocycle Carbenes, Organocatalysis, Asymmetric Synthesis, Dearomatization, 1,4-Dihydropyridine
Organocatalysis
010405 organic chemistry
N-heterocycle Carbenes
Organic Chemistry
Enantioselective synthesis
Ambientale
Regioselectivity
010402 general chemistry
Circular dichroism spectra
01 natural sciences
Medicinal chemistry
0104 chemical sciences
Catalysis
Acylation
Dearomatization
chemistry.chemical_compound
chemistry
Nucleophile
4-Dihydropyridine
Carbene
Asymmetric Synthesis
Subjects
Details
- ISSN :
- 15206904 and 00223263
- Volume :
- 83
- Database :
- OpenAIRE
- Journal :
- The Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....7898081513e3059e652dfdf7aa4def09
- Full Text :
- https://doi.org/10.1021/acs.joc.7b02996