Enhancement of ruthenium-catalyzed olefin metathesis reactions: Searching for new catalyst or new reaction conditions?
✍ Scribed by Szadkowska, Anna; Samojłowicz, Cezary; Grela, Karol
- Book ID
- 118120280
- Publisher
- International Union of Pure and Applied Chemistry
- Year
- 2011
- Tongue
- English
- Weight
- 728 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0033-4545
No coin nor oath required. For personal study only.
✦ Synopsis
Olefin metathesis as a catalytic process constantly gains interest among organic chemists. Over the last decade, it became an efficient tool to accomplish the synthesis of many complex molecules. The development of new well-defined catalysts and continuous examination of novel ligands led to the establishment of metathesis methodology in a group of widespread chemical transformations. Not only does the selection of the catalyst seem to be of crucial importance, but modifying the reaction conditions, such as choice of the solvent and temperature, also allows one to make olefin metathesis a practical industrial process. This contribution, based on examples from our research, is devoted to answering the question “What may have a greater impact on the performance of metathesis reaction: a sophisticated catalyst design or unique reaction conditions?” Based on the data reported in the paper, we discuss two complementary strategies concerning the tuning of the olefin metathesis process.
📜 SIMILAR VOLUMES
## Abstract Four palladium chelate complexes with S‐ or Se‐containing substituted salicylaldehyde Schiff‐base derivatives have been synthesized. Spectroscopic and crystallographic data indicate that, in the complexes, the deprotonated salicylaldehyde ligand is bound to the metal in an O,N,S (or Se)