Synthesis of New Tetrazole Derivatives and Their Biological Evaluation

An operationally simple and efficient method of synthesis of novel 1,5-disubstituted tetrazoles with high yields from easily accessible 2-(2-benzamido-3-arylacrylamido)acetate under mild conditions is developed. Anticancer and anti-microbial tests of the new tetrazole derivatives have been carried o...

Full description

Saved in:
Bibliographic Details
Published in:Russian journal of general chemistry 2018-08, Vol.88 (8), p.1726-1733
Main Authors: Soliman, H. A., Kalmouch, A., Awad, H. M., Abdel Wahed, N. A. M.
Format: Article
Language:English
Subjects:
Acetates
Anti-infective agents
Antiinfectives and antibacterials
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Derivatives
Microorganisms
Peptides
Synthesis
Tetrazoles
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c383t-65b71dbea436f0a693f7c43161509f57e6360a2d77502f651941e2fa640a41893
cites cdi_FETCH-LOGICAL-c383t-65b71dbea436f0a693f7c43161509f57e6360a2d77502f651941e2fa640a41893
container_end_page 1733
container_issue 8
container_start_page 1726
container_title Russian journal of general chemistry
container_volume 88
creator Soliman, H. A.
Kalmouch, A.
Awad, H. M.
Abdel Wahed, N. A. M.
description An operationally simple and efficient method of synthesis of novel 1,5-disubstituted tetrazoles with high yields from easily accessible 2-(2-benzamido-3-arylacrylamido)acetate under mild conditions is developed. Anticancer and anti-microbial tests of the new tetrazole derivatives have been carried out.
doi_str_mv 10.1134/S1070363218080273
format article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_2127695504</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A725791067</galeid><sourcerecordid>A725791067</sourcerecordid><originalsourceid>FETCH-LOGICAL-c383t-65b71dbea436f0a693f7c43161509f57e6360a2d77502f651941e2fa640a41893</originalsourceid><addsrcrecordid>eNp1kU1PwzAMQCsEEmPwA7hV4lywkyZpj3wNkCY4bJyrrHO2oK4ZSTc0fj2ZhjQhQD7Eit-zEzlJzhEuEXl-NUJQwCVnWEABTPGDpIcSioxzAYcxj-VsWz9OTkJ4A0AAyXrJYLRpuzkFG1Jn0mf6SMfUef3pGkrvyNu17uyaQqrbaTqek_XpjXWNm9laN-n9WjerCLj2NDkyugl09n32k9fB_fj2MRu-PDzdXg-zmhe8y6SYKJxOSOdcGtCy5EbVOUeJAkojFEkuQbOpUgKYkQLLHIkZLXPQORYl7ycXu75L795XFLrqza18G0dWDJmSpRCQ76mZbqiyrXHxS_XChrq6VkyoEkGqSF3-QcWY0sLWriVj4_0PAXdC7V0Inky19Hah_aZCqLZbqH5tITps54TItjPy-wf_L30BUkqFRg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2127695504</pqid></control><display><type>article</type><title>Synthesis of New Tetrazole Derivatives and Their Biological Evaluation</title><source>Springer Link</source><creator>Soliman, H. A. ; Kalmouch, A. ; Awad, H. M. ; Abdel Wahed, N. A. M.</creator><creatorcontrib>Soliman, H. A. ; Kalmouch, A. ; Awad, H. M. ; Abdel Wahed, N. A. M.</creatorcontrib><description>An operationally simple and efficient method of synthesis of novel 1,5-disubstituted tetrazoles with high yields from easily accessible 2-(2-benzamido-3-arylacrylamido)acetate under mild conditions is developed. Anticancer and anti-microbial tests of the new tetrazole derivatives have been carried out.</description><identifier>ISSN: 1070-3632</identifier><identifier>EISSN: 1608-3350</identifier><identifier>DOI: 10.1134/S1070363218080273</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Acetates ; Anti-infective agents ; Antiinfectives and antibacterials ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Derivatives ; Microorganisms ; Peptides ; Synthesis ; Tetrazoles</subject><ispartof>Russian journal of general chemistry, 2018-08, Vol.88 (8), p.1726-1733</ispartof><rights>Pleiades Publishing, Ltd. 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Copyright Springer Science &amp; Business Media 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-65b71dbea436f0a693f7c43161509f57e6360a2d77502f651941e2fa640a41893</citedby><cites>FETCH-LOGICAL-c383t-65b71dbea436f0a693f7c43161509f57e6360a2d77502f651941e2fa640a41893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Soliman, H. A.</creatorcontrib><creatorcontrib>Kalmouch, A.</creatorcontrib><creatorcontrib>Awad, H. M.</creatorcontrib><creatorcontrib>Abdel Wahed, N. A. M.</creatorcontrib><title>Synthesis of New Tetrazole Derivatives and Their Biological Evaluation</title><title>Russian journal of general chemistry</title><addtitle>Russ J Gen Chem</addtitle><description>An operationally simple and efficient method of synthesis of novel 1,5-disubstituted tetrazoles with high yields from easily accessible 2-(2-benzamido-3-arylacrylamido)acetate under mild conditions is developed. Anticancer and anti-microbial tests of the new tetrazole derivatives have been carried out.</description><subject>Acetates</subject><subject>Anti-infective agents</subject><subject>Antiinfectives and antibacterials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Derivatives</subject><subject>Microorganisms</subject><subject>Peptides</subject><subject>Synthesis</subject><subject>Tetrazoles</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kU1PwzAMQCsEEmPwA7hV4lywkyZpj3wNkCY4bJyrrHO2oK4ZSTc0fj2ZhjQhQD7Eit-zEzlJzhEuEXl-NUJQwCVnWEABTPGDpIcSioxzAYcxj-VsWz9OTkJ4A0AAyXrJYLRpuzkFG1Jn0mf6SMfUef3pGkrvyNu17uyaQqrbaTqek_XpjXWNm9laN-n9WjerCLj2NDkyugl09n32k9fB_fj2MRu-PDzdXg-zmhe8y6SYKJxOSOdcGtCy5EbVOUeJAkojFEkuQbOpUgKYkQLLHIkZLXPQORYl7ycXu75L795XFLrqza18G0dWDJmSpRCQ76mZbqiyrXHxS_XChrq6VkyoEkGqSF3-QcWY0sLWriVj4_0PAXdC7V0Inky19Hah_aZCqLZbqH5tITps54TItjPy-wf_L30BUkqFRg</recordid><startdate>20180801</startdate><enddate>20180801</enddate><creator>Soliman, H. A.</creator><creator>Kalmouch, A.</creator><creator>Awad, H. M.</creator><creator>Abdel Wahed, N. A. M.</creator><general>Pleiades Publishing</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20180801</creationdate><title>Synthesis of New Tetrazole Derivatives and Their Biological Evaluation</title><author>Soliman, H. A. ; Kalmouch, A. ; Awad, H. M. ; Abdel Wahed, N. A. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-65b71dbea436f0a693f7c43161509f57e6360a2d77502f651941e2fa640a41893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acetates</topic><topic>Anti-infective agents</topic><topic>Antiinfectives and antibacterials</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Derivatives</topic><topic>Microorganisms</topic><topic>Peptides</topic><topic>Synthesis</topic><topic>Tetrazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Soliman, H. A.</creatorcontrib><creatorcontrib>Kalmouch, A.</creatorcontrib><creatorcontrib>Awad, H. M.</creatorcontrib><creatorcontrib>Abdel Wahed, N. A. M.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Soliman, H. A.</au><au>Kalmouch, A.</au><au>Awad, H. M.</au><au>Abdel Wahed, N. A. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of New Tetrazole Derivatives and Their Biological Evaluation</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2018-08-01</date><risdate>2018</risdate><volume>88</volume><issue>8</issue><spage>1726</spage><epage>1733</epage><pages>1726-1733</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>An operationally simple and efficient method of synthesis of novel 1,5-disubstituted tetrazoles with high yields from easily accessible 2-(2-benzamido-3-arylacrylamido)acetate under mild conditions is developed. Anticancer and anti-microbial tests of the new tetrazole derivatives have been carried out.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070363218080273</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1070-3632
ispartof Russian journal of general chemistry, 2018-08, Vol.88 (8), p.1726-1733
issn 1070-3632
1608-3350
language eng
recordid cdi_proquest_journals_2127695504
source Springer Link
subjects Acetates
Anti-infective agents
Antiinfectives and antibacterials
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Derivatives
Microorganisms
Peptides
Synthesis
Tetrazoles
title Synthesis of New Tetrazole Derivatives and Their Biological Evaluation
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T22%3A07%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20New%20Tetrazole%20Derivatives%20and%20Their%20Biological%20Evaluation&rft.jtitle=Russian%20journal%20of%20general%20chemistry&rft.au=Soliman,%20H.%20A.&rft.date=2018-08-01&rft.volume=88&rft.issue=8&rft.spage=1726&rft.epage=1733&rft.pages=1726-1733&rft.issn=1070-3632&rft.eissn=1608-3350&rft_id=info:doi/10.1134/S1070363218080273&rft_dat=%3Cgale_proqu%3EA725791067%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c383t-65b71dbea436f0a693f7c43161509f57e6360a2d77502f651941e2fa640a41893%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2127695504&rft_id=info:pmid/&rft_galeid=A725791067&rfr_iscdi=true