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<ArticleSet>
<Article>
<Journal>
				<PublisherName></PublisherName>
				<JournalTitle>Iranian chemical communication</JournalTitle>
				<Issn>2423-4958</Issn>
				<Volume>3</Volume>
				<Issue>Issue 2, pp. 72-147, Serial No. 7</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Microwave assisted green synthesis of α, ά- bis (substituted- benzylidene) alkanones</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>78</FirstPage>
			<LastPage>85</LastPage>
			<ELocationID EIdType="pii">950</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mohammad Ali</FirstName>
					<LastName>Nasseri</LastName>
<Affiliation>University of Birjand</Affiliation>

</Author>
<Author>
					<FirstName>Ali</FirstName>
					<LastName>Allahresani</LastName>
<Affiliation>Department of Chemistry, College of Sciences, University of Birjand</Affiliation>

</Author>
<Author>
					<FirstName>Batol</FirstName>
					<LastName>Zakeri Nasab</LastName>
<Affiliation>Department of Chemistry, College of Sciences, University of Birjand</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>07</Month>
					<Day>16</Day>
				</PubDate>
			</History>
		<Abstract>Microwave assisted green synthesis of α, ά- bis (substituted- benzylidene) alkanones by the crossed- aldol condensation reaction of substituted aryl aldehydes with ketones in the presence of catalytic amount of NbCl5 in good to excellent yields. This reaction is carried out under solvent-free conditions. The results showed that aldehydes bearing electron–donating substituent&#039;s on phenyl-ring favored the formation of product in good to excellent yields with reaction times ranging between 3 and 7 min. In addition, furfural, cinamaldehyde, thiophene-2-carbaldehyde and 5-methylthiophene-2-carbaldehyde were investigated in aldol reaction, and the results showed excellent yields. Also, the reactions were carried out at room &amp; thermal (80 0C) conditions. The results showed that the yields are in accordance with the microwave irradiations, But the time is 1.5-5 h at room temperature and 15-45 min in thermal conditions.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Niobium pentachloride</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">solvent-free</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Aryl aldehyde</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">microwave irradiation</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://icc.journals.pnu.ac.ir/article_950_42919c08339e12b81fe1aa5e97db66e9.pdf</ArchiveCopySource>
</Article>
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