Synthesis of 2,5-Dihydroisothiazole Derivatives. 2. 3-Aryl(Hetaryl)-Substituted 2-Alkyl-5-Arylimino-2,5-Dihydroisothiazoles

A series of new 2-alkyl-5-arylimino-2,5-dihydroisothiazoles, substituted at position 3 with aryl and hetaryl groups and not substituted at position 4 was prepared by oxidative cyclization of N -arylamides of 3-alkylaminoprop-2-enethioic acids. The formation of the starting thioanilides was investiga...

Full description

Saved in:
Bibliographic Details
Published in:Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2014-04, Vol.50 (1), p.87-102
Main Authors: Skrastiņa, I., Baran, A., Muceniece, D., Popelis, J.
Format: Article
Language:English
Subjects:
Chemistry
Chemistry and Materials Science
Organic Chemistry
Pharmacy
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-c288t-803a2239eacbf4dfad66c9233a198022e74e6a131c5919a00c5202e66896beeb3
cites cdi_FETCH-LOGICAL-c288t-803a2239eacbf4dfad66c9233a198022e74e6a131c5919a00c5202e66896beeb3
container_end_page 102
container_issue 1
container_start_page 87
container_title Chemistry of heterocyclic compounds (New York, N.Y. 1965)
container_volume 50
creator Skrastiņa, I.
Baran, A.
Muceniece, D.
Popelis, J.
description A series of new 2-alkyl-5-arylimino-2,5-dihydroisothiazoles, substituted at position 3 with aryl and hetaryl groups and not substituted at position 4 was prepared by oxidative cyclization of N -arylamides of 3-alkylaminoprop-2-enethioic acids. The formation of the starting thioanilides was investigated by reacting the respective N -alkylimines of acetophenones with isothiocyanates. The main by-products were identified and characterized.
doi_str_mv 10.1007/s10593-014-1451-1
format article
fullrecord <record><control><sourceid>crossref_sprin</sourceid><recordid>TN_cdi_crossref_primary_10_1007_s10593_014_1451_1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1007_s10593_014_1451_1</sourcerecordid><originalsourceid>FETCH-LOGICAL-c288t-803a2239eacbf4dfad66c9233a198022e74e6a131c5919a00c5202e66896beeb3</originalsourceid><addsrcrecordid>eNp9kM9LwzAcxYMoOKd_gLceFczMN2na5jjmjwkDD9NzSNtvXWbXSJINqv-8nfMonh4P3ns8PoRcApsAY_ltACaVoAxSCqkECkdkBDIXtBBSHJMRY0xRAZyfkrMQ1oPNoUhH5GvZd3GFwYbENQm_kfTOrvraOxtcXFnz6VpM7tDbnYl2h2GS8Eki6NT37dUcoxn0mi63ZYg2biPWCafT9r1vqfzJ2I3tHP17NpyTk8a0AS9-dUxeH-5fZnO6eH58mk0XtOJFEWnBhOFcKDRV2aR1Y-osqxQXwoAqGOeYp5gZEFBJBcowVknOOGZZobISsRRjAofdyrsQPDb6w9vNcF0D03t6-kBPD_T0np6GocMPnTBkuzf0eu22vhtu_lP6BkZlcpE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis of 2,5-Dihydroisothiazole Derivatives. 2. 3-Aryl(Hetaryl)-Substituted 2-Alkyl-5-Arylimino-2,5-Dihydroisothiazoles</title><source>Springer Nature:Jisc Collections:Springer Nature Read and Publish 2023-2025: Springer Reading List</source><creator>Skrastiņa, I. ; Baran, A. ; Muceniece, D. ; Popelis, J.</creator><creatorcontrib>Skrastiņa, I. ; Baran, A. ; Muceniece, D. ; Popelis, J.</creatorcontrib><description>A series of new 2-alkyl-5-arylimino-2,5-dihydroisothiazoles, substituted at position 3 with aryl and hetaryl groups and not substituted at position 4 was prepared by oxidative cyclization of N -arylamides of 3-alkylaminoprop-2-enethioic acids. The formation of the starting thioanilides was investigated by reacting the respective N -alkylimines of acetophenones with isothiocyanates. The main by-products were identified and characterized.</description><identifier>ISSN: 0009-3122</identifier><identifier>EISSN: 1573-8353</identifier><identifier>DOI: 10.1007/s10593-014-1451-1</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Chemistry ; Chemistry and Materials Science ; Organic Chemistry ; Pharmacy</subject><ispartof>Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2014-04, Vol.50 (1), p.87-102</ispartof><rights>Springer Science+Business Media New York 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c288t-803a2239eacbf4dfad66c9233a198022e74e6a131c5919a00c5202e66896beeb3</citedby><cites>FETCH-LOGICAL-c288t-803a2239eacbf4dfad66c9233a198022e74e6a131c5919a00c5202e66896beeb3</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>Skrastiņa, I.</creatorcontrib><creatorcontrib>Baran, A.</creatorcontrib><creatorcontrib>Muceniece, D.</creatorcontrib><creatorcontrib>Popelis, J.</creatorcontrib><title>Synthesis of 2,5-Dihydroisothiazole Derivatives. 2. 3-Aryl(Hetaryl)-Substituted 2-Alkyl-5-Arylimino-2,5-Dihydroisothiazoles</title><title>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</title><addtitle>Chem Heterocycl Comp</addtitle><description>A series of new 2-alkyl-5-arylimino-2,5-dihydroisothiazoles, substituted at position 3 with aryl and hetaryl groups and not substituted at position 4 was prepared by oxidative cyclization of N -arylamides of 3-alkylaminoprop-2-enethioic acids. The formation of the starting thioanilides was investigated by reacting the respective N -alkylimines of acetophenones with isothiocyanates. The main by-products were identified and characterized.</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Organic Chemistry</subject><subject>Pharmacy</subject><issn>0009-3122</issn><issn>1573-8353</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9kM9LwzAcxYMoOKd_gLceFczMN2na5jjmjwkDD9NzSNtvXWbXSJINqv-8nfMonh4P3ns8PoRcApsAY_ltACaVoAxSCqkECkdkBDIXtBBSHJMRY0xRAZyfkrMQ1oPNoUhH5GvZd3GFwYbENQm_kfTOrvraOxtcXFnz6VpM7tDbnYl2h2GS8Eki6NT37dUcoxn0mi63ZYg2biPWCafT9r1vqfzJ2I3tHP17NpyTk8a0AS9-dUxeH-5fZnO6eH58mk0XtOJFEWnBhOFcKDRV2aR1Y-osqxQXwoAqGOeYp5gZEFBJBcowVknOOGZZobISsRRjAofdyrsQPDb6w9vNcF0D03t6-kBPD_T0np6GocMPnTBkuzf0eu22vhtu_lP6BkZlcpE</recordid><startdate>20140401</startdate><enddate>20140401</enddate><creator>Skrastiņa, I.</creator><creator>Baran, A.</creator><creator>Muceniece, D.</creator><creator>Popelis, J.</creator><general>Springer US</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20140401</creationdate><title>Synthesis of 2,5-Dihydroisothiazole Derivatives. 2. 3-Aryl(Hetaryl)-Substituted 2-Alkyl-5-Arylimino-2,5-Dihydroisothiazoles</title><author>Skrastiņa, I. ; Baran, A. ; Muceniece, D. ; Popelis, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c288t-803a2239eacbf4dfad66c9233a198022e74e6a131c5919a00c5202e66896beeb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Organic Chemistry</topic><topic>Pharmacy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Skrastiņa, I.</creatorcontrib><creatorcontrib>Baran, A.</creatorcontrib><creatorcontrib>Muceniece, D.</creatorcontrib><creatorcontrib>Popelis, J.</creatorcontrib><collection>CrossRef</collection><jtitle>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Skrastiņa, I.</au><au>Baran, A.</au><au>Muceniece, D.</au><au>Popelis, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of 2,5-Dihydroisothiazole Derivatives. 2. 3-Aryl(Hetaryl)-Substituted 2-Alkyl-5-Arylimino-2,5-Dihydroisothiazoles</atitle><jtitle>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</jtitle><stitle>Chem Heterocycl Comp</stitle><date>2014-04-01</date><risdate>2014</risdate><volume>50</volume><issue>1</issue><spage>87</spage><epage>102</epage><pages>87-102</pages><issn>0009-3122</issn><eissn>1573-8353</eissn><abstract>A series of new 2-alkyl-5-arylimino-2,5-dihydroisothiazoles, substituted at position 3 with aryl and hetaryl groups and not substituted at position 4 was prepared by oxidative cyclization of N -arylamides of 3-alkylaminoprop-2-enethioic acids. The formation of the starting thioanilides was investigated by reacting the respective N -alkylimines of acetophenones with isothiocyanates. The main by-products were identified and characterized.</abstract><cop>Boston</cop><pub>Springer US</pub><doi>10.1007/s10593-014-1451-1</doi><tpages>16</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0009-3122
ispartof Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2014-04, Vol.50 (1), p.87-102
issn 0009-3122
1573-8353
language eng
recordid cdi_crossref_primary_10_1007_s10593_014_1451_1
source Springer Nature:Jisc Collections:Springer Nature Read and Publish 2023-2025: Springer Reading List
subjects Chemistry
Chemistry and Materials Science
Organic Chemistry
Pharmacy
title Synthesis of 2,5-Dihydroisothiazole Derivatives. 2. 3-Aryl(Hetaryl)-Substituted 2-Alkyl-5-Arylimino-2,5-Dihydroisothiazoles
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T16%3A31%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref_sprin&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%202,5-Dihydroisothiazole%20Derivatives.%202.%203-Aryl(Hetaryl)-Substituted%202-Alkyl-5-Arylimino-2,5-Dihydroisothiazoles&rft.jtitle=Chemistry%20of%20heterocyclic%20compounds%20(New%20York,%20N.Y.%201965)&rft.au=Skrasti%C5%86a,%20I.&rft.date=2014-04-01&rft.volume=50&rft.issue=1&rft.spage=87&rft.epage=102&rft.pages=87-102&rft.issn=0009-3122&rft.eissn=1573-8353&rft_id=info:doi/10.1007/s10593-014-1451-1&rft_dat=%3Ccrossref_sprin%3E10_1007_s10593_014_1451_1%3C/crossref_sprin%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c288t-803a2239eacbf4dfad66c9233a198022e74e6a131c5919a00c5202e66896beeb3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true