dc.contributor.advisor | Fiksdahl, Anne | nb_NO |
dc.contributor.author | Rajinder Kaur, Maya | nb_NO |
dc.date.accessioned | 2014-12-19T13:21:46Z | |
dc.date.available | 2014-12-19T13:21:46Z | |
dc.date.created | 2012-11-08 | nb_NO |
dc.date.issued | 2012 | nb_NO |
dc.identifier | 566529 | nb_NO |
dc.identifier | ntnudaim:6967 | nb_NO |
dc.identifier.uri | http://hdl.handle.net/11250/247797 | |
dc.description.abstract | Through this study it has been observed that in contrast to propargyl esters which give cyclopropyl products, the high reactivity of propargyl acetals allows a new tandem cyclization to take place, resulting in bicyclic products. It has also been found that steric effects may cause propargyl acetals to react by unexpected pathways. NMR studies confirmed a particularly high reactivity of propargyl acetal compared to propargyl ester. These results show how molecular diversity can easily be achieved by varying the substrates in gold(I) catalysis. | nb_NO |
dc.language | eng | nb_NO |
dc.publisher | Institutt for kjemi | nb_NO |
dc.subject | ntnudaim:6967 | no_NO |
dc.subject | MTKJ Industriell kjemi og bioteknologi | no_NO |
dc.subject | Organisk kjemi | no_NO |
dc.title | Gold(I) Catalyzed Tandem Cyclization Reactions | nb_NO |
dc.type | Master thesis | nb_NO |
dc.source.pagenumber | 240 | nb_NO |
dc.contributor.department | Norges teknisk-naturvitenskapelige universitet, Fakultet for naturvitenskap og teknologi, Institutt for kjemi | nb_NO |