Browsing by Author "Alshahrani, Nourah Muajeb"
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Item Restricted Studies on Synthesis and Characterizations of Starch Base Copolymers and its Adjustment for Various Industrial Applications(Imam Abdulrahman Bin Faisal University, 2018) Alshahrani, Nourah Muajeb; Abdel-Nabi, Abir; Alghamdi, AzzaIn this research starch graft copolymers were synthesized by free radical polymerization process using potassium persulfate and sodium bisulfate as initiators. Reaction conditions and monomer/initiators ratio were investigated to produce graft copolymers with various molecular weights. Different factors were studied to obtain the optimum grafting conditions. It was found that St-g-DAA produced using water bath gave higher percentage of graft (15.6%) than that produced by ultrasonic waves (9.3%)1 0Item Restricted Transition-metal-free α-arylation of carbonyl compounds via Smiles Rearrangement(The University of Manchester, 2024) Alshahrani, Nourah Muajeb; GreaneyThe Smiles rearrangement, a valuable synthetic tool for constructing complex molecular architectures, has been extensively employed in organic synthesis. In recent years, there has been increased interest in applying the Smiles rearrangement to the arylation of α-carbonyl compounds. We developed a transition metal free alpha arylation of carbonyl compounds via Smiles Rearrangement under mild reaction conditions using: 1- Sulfonates 2- Sulfonamide The use of sulfonates as arylating reagents presents certain limitations, and further investigation is required to improve the efficiency of the rearrangement, which could enhance the overall synthetic pathway. Conversely, sulfonamides have demonstrated potential as effective arylating agents for producing complex molecules under mild conditions. Further exploration is necessary to broaden the scope and optimize conditions to achieve better yields and selectivity. Efforts to achieve asymmetric synthesis of Smiles products from sulfonates were undertaken, but these attempts faced significant challenges, particularly in attaining satisfactory enantioselectivity with the current methodology.11 0