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<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>15</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>2004</Year>
					<Month>09</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Denitration of Nitroesters with Tributyltin Hydride in the Presence of Azobisisobutyronitrile (AIBN)</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31604</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		    <Abstract>Among the different reducing agents tributyltin hydride was found to be a powerful reducing agent for the denitration of a series of tertiary and secondary nitroesters. The organotin residues removed from the crude product using saturated potassium fluoride solution. The yield of the reactions was 62-98%.</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31604_7e64ef4e0d891aed100893d4ba43bb15.pdf</ArchiveCopySource>
</Article>
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