| dc.contributor.author | Malla, Hassan Ali Ahmed | |
| dc.contributor.author | Mossabl, Hamid Adam Mohammed | |
| dc.contributor.author | Supervisor - Ahmed Elsadig Mohammad Saeed | |
| dc.date.accessioned | 2014-12-25T10:05:19Z | |
| dc.date.available | 2014-12-25T10:05:19Z | |
| dc.date.issued | 2014-07-20 | |
| dc.identifier.citation | Malla,Hassan Ali Ahmed.Synthesis of some derivatives of 1,4-Naphthoquinone/Hassan Ali Ahmed Malla,Hamid Adam Mohammed Mossabl;Ahmed Elsadig Mohammad Saeed.-khartoum:Sudan University of Science and Technology,College of Science,2014.-36p. :ill;28cm.-Basheors,search . | en_US | 
| dc.identifier.uri | http://repository.sustech.edu/handle/123456789/9250 | |
| dc.description | Basheors,search | en_US | 
| dc.description.abstract | In this work, 2–{5–[(2–phenylhydrazinylidene)methyl] furan–2–yl}naphthalene-1,4-dione and 2–{4-[(2– phenylhydrazinyliden)methyl]phenyl}naphthalene-1,4-dione have been synthesized by reaction of 1-(furan-2-ylmethlidene)- 2-phenylhydrazine and 1-benzylidene-2-phenylhydrazine as hydrazones with 1,4-naphthoquinone according to a well documented procedure. Access to furylnaphthoquinones from un activated quinones requires acid-inuced conditions, however oxidation coupling reaction of activated quinones proceed under neutral condition. The hydrazones were prepared from the commercially aldehydes and phenyl hydrazine. | en_US | 
| dc.description.sponsorship | Sudan University of Science and Technology | en_US | 
| dc.language.iso | en | en_US | 
| dc.publisher | Sudan University of Science and Technology | en_US | 
| dc.subject | Chemical Science | en_US | 
| dc.subject | Synthesis of some derivatives | en_US | 
| dc.subject | Naphthoquinone | en_US | 
| dc.subject | Oxidation reaction | en_US | 
| dc.title | Synthesis of some derivatives of 1,4-Naphthoquinone | en_US | 
| dc.type | Thesis | en_US |