<?xml version="1.0" encoding="UTF-8"?>
<!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>9</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>1998</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>SYNTHESES, ANTIFUNGAL AND
ANTIBACTERIAL ACTIVITIES OF
SUBSTITUTED 1,2, CTRIMOLES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31362</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		    <Abstract>The reaction of readily available 1 -methyl-4-nitropyrrole-2- carboxylic acid (1)
with thionyl chloride afforded the corresponding acyl chloride 2. The reaction of
compound 2 with thiosemicarbazides yielded 1-(1 -methyl-4-nitrop yrrole-2-carbony1)-
thiosemicarbazides (3) which cyclized in basic medium to 5-(1-methyl-4-nitropyrrole-
2-y1)-2,4-dihydro-3H- l,2,4-triazole-3- thione 4. Alkylation and subsequent oxidation
of 4 gave 6. The antibacterial and antifungal activities of 6a to 6f against a number
of microorganisms were determined. Only compounds 6b and 6c had moderate
activity against Aspergilus niger</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31362_be6534833d70c9056185831475fd92a1.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
