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 |