Please use this identifier to cite or link to this item: https://repository.seku.ac.ke/handle/123456789/2667
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dc.contributor.authorMusau, Peter-
dc.contributor.authorBrian, Ptoton M.-
dc.date.accessioned2016-09-30T09:13:47Z-
dc.date.available2016-09-30T09:13:47Z-
dc.date.issued2016-
dc.identifier.citationIndonesian journal of chemistry: Vol 16, No 1en_US
dc.identifier.urihttp://pdm-mipa.ugm.ac.id/ojs/index.php/ijc/article/view/1042/1158-
dc.identifier.urihttp://repository.seku.ac.ke/handle/123456789/2667-
dc.description.abstractThis paper reports the synthesis and reactivity of different Benzyl derivative protecting groups. The synthesis and stability of Benzyl halides, 4-methoxybenzyl halides, 3,5-dimethoxybenzyl halides, 3,4-dimethoxybenzyl halides, 3,4,5-trimethoxybenzyl halide protecting groups and their reactivity towards nitrogen atom of a di-substituted pyridine ring in formation of pyridinium salts is also reported.en_US
dc.language.isoenen_US
dc.subjectaryl halide protecting groupsen_US
dc.subjectbenzyl halidesen_US
dc.subject4-methoxybenzyl halideen_US
dc.subject3,5-dimethoxybenzyl halideen_US
dc.subject3,4- dimethoxybenzyl halideen_US
dc.titleSynthesis, reactivity and stability of aryl halide protecting groups towards di-substituted pyridinesen_US
dc.typeArticleen_US
Appears in Collections:School of Science and Computing (JA)



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