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Enantioselective Divergent Synthesis of C19-Oxo Eburnane Alkaloids via Palladium-Catalyzed Asymmetric Allylic Alkylation of an N-Alkyl-α,β-unsaturated Lactam
- Source :
- Journal of the American Chemical Society. 141(12)
- Publication Year :
- 2019
-
Abstract
- The C19-oxo-functionalized eburnane alkaloids display unique chemical structure and interesting biological activity. Herein, we report a divergent enantioselective strategy to access these alkaloids by use of a challenging palladium-catalyzed asymmetric allylic alkylation of an N-alkyl-α,β-unsaturated lactam. 19-( S)-OH-Δ
- Subjects :
- chemistry.chemical_classification
Chemistry
Stereochemistry
Chemical structure
Enantioselective synthesis
chemistry.chemical_element
General Chemistry
010402 general chemistry
01 natural sciences
Biochemistry
Catalysis
0104 chemical sciences
chemistry.chemical_compound
Tsuji–Trost reaction
Colloid and Surface Chemistry
Lactam
Divergent synthesis
Alkyl
Palladium
Subjects
Details
- ISSN :
- 15205126
- Volume :
- 141
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- Journal of the American Chemical Society
- Accession number :
- edsair.doi.dedup.....12fead32b1145c0d3bfe5b1ff1ac7425