Application of chiral schiff bases of cu complexes in the asymmetric nitro aldol reactions
2007
0 views
0 downloads
Advisor: Doç.dr. Nadir Demirel
Abstract (EN)
The nitroaldol reaction (or Henry reaction) is one of themost important and atom-economical reactions for carbon?carbon bond formation to generate bnitroalkanols. The diversity of the transformation of adducts, such as reduction to amines, Nef reaction to carbonyl compounds, or dehydration to nitroalkenes, offers avariety of applications for this reaction. Recent effortshave been focused on the development of catalytic enantioselective reaction variants. In these processes, differentchiral catalysts were developed, such as thosebased upon BINOL by Shibasaki, Bis(oxazoline) by Evans and Jørgensen, cinchona alkaloid by Corey, dinuclear zinc complexes by Trost, Salen?Co complexes by Yamada, and amino alcohols by Palomo.
Author
Dr. Mehmet Çolak
How to Cite
Mehmet Çolak (Master Thesis). Application of chiral schiff bases of cu complexes in the asymmetric nitro aldol reactions, 2007, Dicle University.
Keywords
License
Tüm Hakları Saklıdır
This work is shared under the specified license terms.
More theses from Dicle University
- Resilience based design of rc buildings using seismic fragility analyses and a novel wall model(2023)
- The role of financial architecture and institutional structure in growth and development: The example Diyarbakır(2023)
- Determination of neuromarkers associated with dementia using EEG and machine learning(2023)
- Forensic medical examination of earthquake victims admitted to Dicle universi̇tesi Medical Faculty Hospitals as a result of the 6 february 2023 Kahramanmaraş centered earthquakes(2024)
- STEAM in geography education and sample applications(2024)
- Determination of forage quality characteristics of some trigonella genotypes growing in meadow-pasture and natural vegetation of southeastern anatolia region(2024)
