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Asymmetric Synthesis of α-Alkylidene-β-Lactams through Copper Catalysis with a Prolinol-Phosphine Chiral Ligand
- Source :
- Organic letters. 21(6)
- Publication Year :
- 2019
-
Abstract
- A copper/prolinol-phosphine chiral catalyst enabled the one-step synthesis of chiral α-alkylidene-β-lactams. Optimization of the chiral ligand for steric and electronic properties realized the highly enantioselective coupling of nitrones and propargyl alcohol derived alkynes. The resulting chiral α-alkylidene-β-lactams served as a platform for various β-lactams via well-established transformations of α,β-unsaturated carbonyl compounds.
- Subjects :
- Steric effects
010405 organic chemistry
Chemistry
Organic Chemistry
Chiral ligand
Enantioselective synthesis
chemistry.chemical_element
Propargyl alcohol
010402 general chemistry
01 natural sciences
Biochemistry
Copper
Combinatorial chemistry
0104 chemical sciences
Catalysis
Prolinol
chemistry.chemical_compound
Physical and Theoretical Chemistry
Phosphine
Subjects
Details
- ISSN :
- 15237052
- Volume :
- 21
- Issue :
- 6
- Database :
- OpenAIRE
- Journal :
- Organic letters
- Accession number :
- edsair.doi.dedup.....af16b116a3d1c2181ebd227ece7a2608