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NHC Backbone Configuration in Ruthenium-Catalyzed Olefin Metathesis
- Source :
- Molecules, Molecules, Vol 21, Iss 1, p 117 (2016)
- Publication Year :
- 2016
- Publisher :
- MDPI, 2016.
-
Abstract
- The catalytic properties of olefin metathesis ruthenium complexes bearing N-heterocyclic carbene ligands with stereogenic centers on the backbone are described. Differences in catalytic behavior depending on the backbone configurations of symmetrical and unsymmetrical NHCs are discussed. In addition, an overview on asymmetric olefin metathesis promoted by chiral catalysts bearing C₂-symmetric and C₁-symmetric NHCs is provided.
- Subjects :
- NHC ligands
Pharmaceutical Science
chemistry.chemical_element
stereogenic centers
Review
Alkenes
010402 general chemistry
Metathesis
Ligands
01 natural sciences
Catalysis
Ruthenium
Analytical Chemistry
Stereocenter
lcsh:QD241-441
chemistry.chemical_compound
lcsh:Organic chemistry
Drug Discovery
Ring-opening metathesis polymerisation
Physical and Theoretical Chemistry
Ruthenium catalysts
Stereogenic centers
Methane
Molecular Structure
Medicine (all)
Organic Chemistry
Olefin metathesis
010405 organic chemistry
Chemistry
Combinatorial chemistry
0104 chemical sciences
Chemistry (miscellaneous)
Molecular Medicine
metathesis
Carbene
Acyclic diene metathesis
ruthenium catalysts
Subjects
Details
- Language :
- English
- ISSN :
- 14203049
- Volume :
- 21
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Molecules
- Accession number :
- edsair.doi.dedup.....95ac5e46122437d68e07e2f2d9d009e5