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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>1</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>1990</Year>
					<Month>08</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SELENIUM HETEROCYCLES XXXX [I]
SYNTHESES OF 4- (2-PYRAZINYL) - 1, 2, 3:
SELENADIAZOLE AND 4- (2-PYRAZILYL)&#039; -
l,2,3- THIADIAZOLE</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31458</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		    <Abstract>Reaction of thionyl chloride with 2-acetyl-1- benzenesulfonylpyrrole semicarbazone
(6 c) gave 4 - (1- benzenesulfonyl-2 - pyrrolyl) - 1, 2, 3 -thiadiazole (lc).
Selenium dioxide oxidation of 2-acetylpyrazine semicarbazone (10) in acetic acid
afforded 4- (2-pyrazinyl) - 1, 2, 3- selenadiazole (4). Reaction of thionyl chloride
with compound 10 gave 4- (2-pyrazinyl) - 1, 2, 3- thiadiazole (3). Base catalized
decomposition of 4 afforded the cis-fulvene 13. Similarly, reaction of 3 with a base
gave the corresponding cis-fulvene 11. Heating compounds 11 or 13 gave
respectively the corresponding trans isomers 12 or 14.</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31458_35e70893fec54c27bc46a147e73aa552.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
