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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<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>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>1999</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SELECTIVE CYCLIZATION AND
IS OMERIZATION OF 3-PROPARGYLTHIO- 1,2,4-
BENZOTRIAZINE TO THIAZOLO [2,3-C] [1,2,4]
BENZOTRIAZINE</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31347</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		    <Abstract>The method cited in the literature for synthesis of 1,2- dihydro 3- thioxo - 1,2,4-
benzotriazine 1 was improved .1 was condensed with propargyl bromide to afford 3 - propargylthio – 1,2,4 -benzotriazine 5.  Transformation of this compound to 9H-3- 
methylthiazolo  [2,3-c] [1,2,4] benzotriazine ( 3, R = Me) was performed in the presence of Na  O   Me / MeOH  . Orientation of this selective cyclization was ascertained by  (N.O.E.) NMR experiment</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31347_fbdf42a1e05260c8a58057ed7e2eb77b.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
