Show simple item record

dc.contributor.authorWanekaya, Adam K
dc.date.accessioned2013-05-09T06:32:46Z
dc.date.available2013-05-09T06:32:46Z
dc.date.issued1993
dc.identifier.citationM.Sc. Thesisen
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/20508
dc.descriptionMaster of Science Thesisen
dc.description.abstractA kinetic study of acid-catalysed rearrangement of 6-ethoxy-5,6- dihydro-3-para-substituted phenyl-4H-l ,2-oxazines (9) in methanol (MeOH), cyanomethane (MeCN) and in dimethylsulfoxide (M~SO) to 3,4-dihydro-2- methoxy-5-parasubstituted phenyl-2H-pyrrole-l-oxides (10) is reported. The substrate oxazines were synthesized by the cycioaddition reaction of 2- bromopara-substituted acetophenone oximes with ethyl vinyl ether in dichloromethane..............
dc.description.sponsorshipUniversity of Nairobien
dc.language.isoenen
dc.titleKinetic study of acid-catalysed rearrangements of 1,2-oxazinesen
dc.typeThesisen
local.publisherDepatment of Chemistry, University of Nairobien


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record