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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>10</Volume>
				<Issue>3</Issue>
				<PubDate PubStatus="epublish">
					<Year>1999</Year>
					<Month>09</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SYNTHESIS OF NORBORNENE FURYL ESTERS
AND THEIR ENZYMATIC KINETIC
RESOLUTION BY PIG LIVER ESTRASE (PLE)</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31432</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		    <Abstract>The reaction of furylacrylic acid with cyclopentadiene in toluene gave the
expected Diels-Alder endo-and exo-adductsin -1 : 1 ratio. The adducts were separated
by iodolactonization method to provide 3-endo-(2&#039;-furyl) bicyclo 12.2.11 hept-5-ene-
2-exo-carboxylic acid and 3-exo-(2&#039;-fury1)bicyclo 12.2.11 hept-5-ene-2-endocarboxylic
acid. Esterification of these acids by MeI / HMPA gave the expected
methyl esters. Kinetic resolution of racemic endo- and exo-ester adducts by
PLE(phosphate buffer, pH, 8) provided the related optically active isomers</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31432_9802a535bbdbcec203871db6d9595586.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
