3-Alkyl-2-phenyl-1-vinylpyrroles from ketoximes and acetylene: an improved synthesis by the Trofimov reaction

A one-pot synthesis of 3-alkyl-2-phenyl-1-vinylpyrroles, giving high yields at atmospheric pressure, was developed on the basis of reacting alkyl phenyl ketoximes with acetylene in a KOH–DMSO system (the Trofimov reaction).

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2013-02, Vol.48 (11), p.1628-1633
Hauptverfasser:	Petrova, O. V., Sobenina, L. N., Mikhaleva, A. I.
Format:	Artikel
Sprache:	eng
Schlagworte:	Acetylene Chemistry Chemistry and Materials Science Organic Chemistry Pharmacy
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

container_end_page	1633
container_issue	11
container_start_page	1628
container_title	Chemistry of heterocyclic compounds (New York, N.Y. 1965)
container_volume	48
creator	Petrova, O. V. Sobenina, L. N. Mikhaleva, A. I.
description	A one-pot synthesis of 3-alkyl-2-phenyl-1-vinylpyrroles, giving high yields at atmospheric pressure, was developed on the basis of reacting alkyl phenyl ketoximes with acetylene in a KOH–DMSO system (the Trofimov reaction).
doi_str_mv	10.1007/s10593-013-1184-6
format	Article
fullrecord	<record><control><sourceid>gale_cross</sourceid><recordid>TN_cdi_gale_infotracacademiconefile_A335292591</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A335292591</galeid><sourcerecordid>A335292591</sourcerecordid><originalsourceid>FETCH-LOGICAL-c327t-73981423b83829f2fe53b9e40a20518a19136aa44eb0f2a577a621cad4863ed63</originalsourceid><addsrcrecordid>eNp9UMtOwzAQtBBIlMIHcPMPuNjePLlVFS-pEpdyttxk3bpN7MoOFfl7XIUz2sPOrGZ2tUPIo-ALwXn5FAXPa2BcABOiylhxRWYiL4FVkMM1mXHOawZCyltyF-Mh0TLJZqQHtuyOY8ckO-3RJSDY2aZ-GkPwHUZqgu_pEQf_Y_tEtWupbnAYO3T4nCi1_Sn4M7Y0jm7YY7SRbkeaEN0Eb2zvzzSgbgbr3T25MbqL-PDX5-Tr9WWzemfrz7eP1XLNGpDlwEqoK5FJ2FZQydpIgzlsa8y4ljwXlRa1gELrLMMtN1LnZakLKRrdZlUB2BYwJ4tp7053qKwzfgi6SdVibxvv0Ng0XwLkspZ52jYnYjI0wccY0KhTsL0OoxJcXQJWU8AqBawuAavLETl5YtK6HQZ18N_Bpb_-Mf0CrY9-bQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>3-Alkyl-2-phenyl-1-vinylpyrroles from ketoximes and acetylene: an improved synthesis by the Trofimov reaction</title><source>Springer Nature - Complete Springer Journals</source><creator>Petrova, O. V. ; Sobenina, L. N. ; Mikhaleva, A. I.</creator><creatorcontrib>Petrova, O. V. ; Sobenina, L. N. ; Mikhaleva, A. I.</creatorcontrib><description>A one-pot synthesis of 3-alkyl-2-phenyl-1-vinylpyrroles, giving high yields at atmospheric pressure, was developed on the basis of reacting alkyl phenyl ketoximes with acetylene in a KOH–DMSO system (the Trofimov reaction).</description><identifier>ISSN: 0009-3122</identifier><identifier>EISSN: 1573-8353</identifier><identifier>DOI: 10.1007/s10593-013-1184-6</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Acetylene ; Chemistry ; Chemistry and Materials Science ; Organic Chemistry ; Pharmacy</subject><ispartof>Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2013-02, Vol.48 (11), p.1628-1633</ispartof><rights>Springer Science+Business Media New York 2013</rights><rights>COPYRIGHT 2013 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-73981423b83829f2fe53b9e40a20518a19136aa44eb0f2a577a621cad4863ed63</citedby><cites>FETCH-LOGICAL-c327t-73981423b83829f2fe53b9e40a20518a19136aa44eb0f2a577a621cad4863ed63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10593-013-1184-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10593-013-1184-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27915,27916,41479,42548,51310</link.rule.ids></links><search><creatorcontrib>Petrova, O. V.</creatorcontrib><creatorcontrib>Sobenina, L. N.</creatorcontrib><creatorcontrib>Mikhaleva, A. I.</creatorcontrib><title>3-Alkyl-2-phenyl-1-vinylpyrroles from ketoximes and acetylene: an improved synthesis by the Trofimov reaction</title><title>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</title><addtitle>Chem Heterocycl Comp</addtitle><description>A one-pot synthesis of 3-alkyl-2-phenyl-1-vinylpyrroles, giving high yields at atmospheric pressure, was developed on the basis of reacting alkyl phenyl ketoximes with acetylene in a KOH–DMSO system (the Trofimov reaction).</description><subject>Acetylene</subject><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>2013</creationdate><recordtype>article</recordtype><recordid>eNp9UMtOwzAQtBBIlMIHcPMPuNjePLlVFS-pEpdyttxk3bpN7MoOFfl7XIUz2sPOrGZ2tUPIo-ALwXn5FAXPa2BcABOiylhxRWYiL4FVkMM1mXHOawZCyltyF-Mh0TLJZqQHtuyOY8ckO-3RJSDY2aZ-GkPwHUZqgu_pEQf_Y_tEtWupbnAYO3T4nCi1_Sn4M7Y0jm7YY7SRbkeaEN0Eb2zvzzSgbgbr3T25MbqL-PDX5-Tr9WWzemfrz7eP1XLNGpDlwEqoK5FJ2FZQydpIgzlsa8y4ljwXlRa1gELrLMMtN1LnZakLKRrdZlUB2BYwJ4tp7053qKwzfgi6SdVibxvv0Ng0XwLkspZ52jYnYjI0wccY0KhTsL0OoxJcXQJWU8AqBawuAavLETl5YtK6HQZ18N_Bpb_-Mf0CrY9-bQ</recordid><startdate>20130201</startdate><enddate>20130201</enddate><creator>Petrova, O. V.</creator><creator>Sobenina, L. N.</creator><creator>Mikhaleva, A. I.</creator><general>Springer US</general><general>Springer</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20130201</creationdate><title>3-Alkyl-2-phenyl-1-vinylpyrroles from ketoximes and acetylene: an improved synthesis by the Trofimov reaction</title><author>Petrova, O. V. ; Sobenina, L. N. ; Mikhaleva, A. I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c327t-73981423b83829f2fe53b9e40a20518a19136aa44eb0f2a577a621cad4863ed63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Acetylene</topic><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>Petrova, O. V.</creatorcontrib><creatorcontrib>Sobenina, L. N.</creatorcontrib><creatorcontrib>Mikhaleva, A. I.</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>Petrova, O. V.</au><au>Sobenina, L. N.</au><au>Mikhaleva, A. I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>3-Alkyl-2-phenyl-1-vinylpyrroles from ketoximes and acetylene: an improved synthesis by the Trofimov reaction</atitle><jtitle>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</jtitle><stitle>Chem Heterocycl Comp</stitle><date>2013-02-01</date><risdate>2013</risdate><volume>48</volume><issue>11</issue><spage>1628</spage><epage>1633</epage><pages>1628-1633</pages><issn>0009-3122</issn><eissn>1573-8353</eissn><abstract>A one-pot synthesis of 3-alkyl-2-phenyl-1-vinylpyrroles, giving high yields at atmospheric pressure, was developed on the basis of reacting alkyl phenyl ketoximes with acetylene in a KOH–DMSO system (the Trofimov reaction).</abstract><cop>Boston</cop><pub>Springer US</pub><doi>10.1007/s10593-013-1184-6</doi><tpages>6</tpages></addata></record>
fulltext	fulltext
identifier	ISSN: 0009-3122
ispartof	Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2013-02, Vol.48 (11), p.1628-1633
issn	0009-3122 1573-8353
language	eng
recordid	cdi_gale_infotracacademiconefile_A335292591
source	Springer Nature - Complete Springer Journals
subjects	Acetylene Chemistry Chemistry and Materials Science Organic Chemistry Pharmacy
title	3-Alkyl-2-phenyl-1-vinylpyrroles from ketoximes and acetylene: an improved synthesis by the Trofimov reaction
url	https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T06%3A59%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=3-Alkyl-2-phenyl-1-vinylpyrroles%20from%20ketoximes%20and%20acetylene:%20an%20improved%20synthesis%20by%20the%20Trofimov%20reaction&rft.jtitle=Chemistry%20of%20heterocyclic%20compounds%20(New%20York,%20N.Y.%201965)&rft.au=Petrova,%20O.%20V.&rft.date=2013-02-01&rft.volume=48&rft.issue=11&rft.spage=1628&rft.epage=1633&rft.pages=1628-1633&rft.issn=0009-3122&rft.eissn=1573-8353&rft_id=info:doi/10.1007/s10593-013-1184-6&rft_dat=%3Cgale_cross%3EA335292591%3C/gale_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_galeid=A335292591&rfr_iscdi=true