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Stereoretentive Olefin Metathesis: An Avenue to Kinetic Selectivity
- Publication Year :
- 2017
- Publisher :
- Wiley, 2017.
-
Abstract
- Olefin metathesis is an incredibly valuable transformation that has gained widespread use in both academic and industrial settings. Lately, stereoretentive olefin metathesis has garnered much attention as a method for the selective generation of both E- and Z-olefins. Early studies employing ill-defined catalysts showed evidence for retention of the stereochemistry of the starting olefins at low conversion. However, thermodynamic ratios E/Z were reached as the reaction proceeded to equilibrium. Recent studies in olefin metathesis have focused on the synthesis of catalysts that can overcome the inherent thermodynamic preference of an olefin, providing synthetically useful quantities of a kinetically favored olefin isomer. These reports have led to the development of stereoretentive catalysts that not only generate Z-olefins selectively, but also kinetically produce E-olefins, a previously unmet challenge in olefin metathesis. Advancements in stereoretentive olefin metathesis using tungsten, ruthenium, and molybdenum catalysts are presented.
- Subjects :
- Molybdenum
Olefin fiber
Olefin metathesis
Molecular Structure
010405 organic chemistry
Chemistry
chemistry.chemical_element
Stereoisomerism
General Chemistry
Alkenes
010402 general chemistry
01 natural sciences
Catalysis
Ruthenium
Tungsten
0104 chemical sciences
Kinetics
Organic chemistry
Ring-opening metathesis polymerisation
Selectivity
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....3203bc6db07f543c237a9d82a8954cd4