Cinchona Alkaloids in Synthesis and Catalysis: Ligands, Immobilization and Organocatalysis

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One-Pot Diastereoselective Synthesis of Azabicyclo[2.2.2]octanes

Article Views Altmetric -. Citations 2. Note: In lieu of an abstract, this is the article's first page.


  • Choong Eui Song - Google Scholar Citations?
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Cited By. This article is cited by 1 publications. Michael H.

Wang, Daniel T. Cohen, C. The products were unambiguously identified using NMR and IR spectroscopy as well as mass spectrometry and, for one example, by X-ray diffraction analysis.

Lecture Catalytic Organometallics 27 Prof G Dyker 150714

The starting benzalacetones are easily synthesized from benzaldehyde and acetone C. Conard, M.


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  • Cinchona Alkaloids in Synthesis and Catalysis : Ligands, Immobilization and Organocatalysis.

Dolliver Org. The method was optimized with respect to solvent, temperature and base, and the substrate scope was modestly examined using electron-rich and electron-poor aromatic substitution.

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The electronics of the ring had surprisingly little effect on the yield of the reaction; however, ortho -substituted dibenzalacetones did not provide products, probably due to steric hindrance effects. Andrews 23 September : This latest comprehensive reference set on spectroscopy and spectrometers systematically covers the theory, hardware and applications. Cinchona Alkaloids in Synthesis and Catalysis: Ligands, Immobilization and Organocatalysis Author: Choong Eui Song 23 September : This comprehensive review of cinchona-based chiralilty inducers and their applications covers every topic, including ligands, immobilization and organocatalysis.

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