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<ArticleSet>
<Article>
<Journal>
				<PublisherName>Sharif University of Technology</PublisherName>
				<JournalTitle>Scientia Iranica</JournalTitle>
				<Issn>1026-3098</Issn>
				<Volume>21</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>2014</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>An efficient synthesis of monoarylidene derivatives of pyran-4-one and piperidin-4-one</ArticleTitle>
<VernacularTitle>An efficient synthesis of monoarylidene derivatives of pyran-4-one and piperidin-4-one</VernacularTitle>
			<FirstPage>719</FirstPage>
			<LastPage>726</LastPage>
			<ELocationID EIdType="pii">3510</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mohammad M.</FirstName>
					<LastName>Mojtahedi</LastName>
<Affiliation>Chemistry and Chemical Engineering Research Center of Iran P.O.Box 14335-186, ‎Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>M. Saeed</FirstName>
					<LastName>Abaee</LastName>
<Affiliation>Chemistry and Chemical Engineering Research Center of Iran P.O.Box 14335-186, ‎Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Maedeh</FirstName>
					<LastName>Samianifard</LastName>
<Affiliation>Chemistry and Chemical Engineering Research Center of Iran P.O.Box 14335-186, ‎Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Akram</FirstName>
					<LastName>Shamloo</LastName>
<Affiliation>Chemistry and Chemical Engineering Research Center of Iran P.O.Box 14335-186, ‎Tehran, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>02</Month>
					<Day>23</Day>
				</PubDate>
			</History>
		<Abstract>A room-temperature procedure is developed for the direct synthesis of monoarylidene derivatives of pyran-4-one and piperidin-4-one systems under solvent-free conditions. Relatively high yields of products are obtained from the reaction of ketones 1 with different aromatic and aliphatic aldehydes under the catalytic system of TMSNMe2 and MgBr2·OEt2. Notably, formation of the undesired bis counterparts as a major limitation of these reaction types, is minimized using the employed conditions.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">a,b-Unsaturated ketones</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Organocatalysis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Heterocyclic chemistry</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Aldol condensation</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://scientiairanica.sharif.edu/article_3510_15e122e839dfdaa7ce969536f94aecf6.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
