Moleele, Simon Sana2008-03-192008-03-192008-03-19http://hdl.handle.net/10539/4688Abstract This thesis is divided into two parts. Part one presents a novel method for the synthesis of naphthalenes bearing aryl substituents. The novel route starts from three simple and readily available tetralones, α-tetralone, 6-methoxy-α-tetralone and 6,7-dimethoxy-α- tetralone. By means of standard Suzuki coupling methodology and aromatization methods, twelve aryl-substituted naphthalenes were synthesized from the tetralones over five steps in good yields. Some of the aryl-substituted naphthalenes synthesized have shown positive results when tested against malignant cancer cells. Part one also explains how unexpected cyclopropa[a]naphthalenes were obtained from 1-aryl-3,4-dihydro-2- naphthaldehydes by treatment with lithium aluminium hydride. The methodology developed in part one is further explored in part two of the thesis, which describes the synthesis of analogues of [1,1’]binaphthalenyl-2,2’-diol. A small library of twelve different biaryl diols was prepared from simple bromo(methoxy)naphthaldehydes that were synthesized in part one. The resultant biaryl diols were used in the design of twenty-two novel phosphite, phosphate, phosphoramidite and phosphoramidate ligands in which the phosphorus atoms are contained in either a nine-or an eight-membered heteroatom ring. However, these ligands are still to be tested in metal-catalyzed hydrogenation reactions.2994562 bytes73878 bytesapplication/pdfapplication/pdfennaphthalenesphosphitesphosphoramiditescatalysisThesis