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	<Article> 

	<Journal> 

	<PublisherName>International Science Community Association</PublisherName>

	<JournalTitle>Research Journal of Chemical Sciences</JournalTitle> 

	<Issn>2231 - 606X</Issn>

	<Volume>5</Volume>

	<Issue>6</Issue>

	<PubDate PubStatus="ppublish"> 

	<Year>2015</Year> 

	<Month>June</Month> 

	<Day>18</Day> 

	</PubDate>

	</Journal>



	<ArticleTitle>Synthesis of New Seleno-nitrone Compounds</ArticleTitle> 


	<FirstPage>5</FirstPage>

	<LastPage>8</LastPage>



	<ELocationID EIdType="pii"></ELocationID>

	<Language>EN</Language> 
	<AuthorList>

	
		<Author> 

		<FirstName>Chauhan</FirstName>

		<MiddleName> </MiddleName>

		<LastName>Sumedha</LastName>

		<Suffix>1</Suffix>

		<Affiliation></Affiliation>

		</Author>
		<Author> 

		<FirstName>Yadav</FirstName>

		<MiddleName> </MiddleName>

		<LastName>S.S.</LastName>

		<Suffix>2</Suffix>

		<Affiliation></Affiliation>

		</Author>
		<Author> 

		<FirstName>HaddadBatool</FirstName>

		<MiddleName> </MiddleName>

		<LastName>S.</LastName>

		<Suffix>1</Suffix>

		<Affiliation> Department of chemistry, college of Science, University of Basrah, Basrah, IRAQ</Affiliation>

		</Author>
		<Author> 

		<FirstName>MajeedNisreen</FirstName>

		<MiddleName> </MiddleName>

		<LastName>N.</LastName>

		<Suffix>2</Suffix>

		<Affiliation></Affiliation>

		</Author>
		<Author> 

		<FirstName>Al-RubaieAli</FirstName>

		<MiddleName> </MiddleName>

		<LastName>Z.</LastName>

		<Suffix>3</Suffix>

		<Affiliation></Affiliation>

		</Author>

	<Author>

	<CollectiveName></CollectiveName>>

	</Author>

	</AuthorList>


	<PublicationType>Research Paper</PublicationType>


	<History>  
	<PubDate PubStatus="received">
	<Year>2015</Year>
	<Month>5</Month>
	<Day>9</Day>
	</PubDate>
	<PubDate PubStatus="accepted">										
	<Year>2015</Year> 
	<Month>June</Month>									
	<Day>18</Day> 
	</PubDate>

	</History>
	<Abstract>The 1,1-Diiodo-1-seleno-4-cyclohexanone were synthesized from the reaction of 1,1-Dibromo-3-penta-none with selenium and then converted to nitrones by the condensation of carbonyl group with substituted N-phenylhydroxylamine. The resulting products were identified by physical properties such as melting poin (m.p.), retardation factor (Rf) and color. Also compounds showed the expected data in identification techniques such as FTIR, HNMR, mass spectroscopy and Elemental analysis (CHN). The results proved the validity of the expected chemical structures of synthesized compounds.</Abstract>

	<CopyrightInformation>Copyright@ International Science Community Association</CopyrightInformation>

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