Synthesis and chemistry of new spiro‐Δ 1 ‐pyrazoline
In explorations of syntheses and chemistry of spiroheterocycles, we found that the reaction of 2‐diazopropane with ( E )‐α‐arylidenepyrrolin‐2‐one, ( E )‐α‐arylidene‐γ‐butyrolactone, and ( E )‐arylidene‐ N ‐arylsuccinimide derivatives produced spiro‐Δ 1 ‐pyrazolines. The photolysis of Δ 1 ‐pyrazolin...
Gespeichert in:
| Veröffentlicht in: | Journal of heterocyclic chemistry 2012-03, Vol.49 (2), p.267-271 |
|---|---|
| Hauptverfasser: | , , , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 271 |
|---|---|
| container_issue | 2 |
| container_start_page | 267 |
| container_title | Journal of heterocyclic chemistry |
| container_volume | 49 |
| creator | Louhichi, Nesrine Houas, Amel Hamadi, Naoufel Ben Msaddek, Moncef |
| description | In explorations of syntheses and chemistry of spiroheterocycles, we found that the reaction of 2‐diazopropane with (
E
)‐α‐arylidenepyrrolin‐2‐one, (
E
)‐α‐arylidene‐γ‐butyrolactone, and (
E
)‐arylidene‐
N
‐arylsuccinimide derivatives produced spiro‐Δ
1
‐pyrazolines. The photolysis of Δ
1
‐pyrazolines has led to cyclopropanes. The structures of the obtained adducts have been assigned by means of spectroscopic measurements. J. Heterocyclic Chem., (2011). |
| doi_str_mv | 10.1002/jhet.827 |
| format | Article |
| fullrecord | <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1002_jhet_827</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1002_jhet_827</sourcerecordid><originalsourceid>FETCH-LOGICAL-c727-92cfacff69379ad9a21cbcf4333158a01714e6e6e083c46411b49297240673d83</originalsourceid><addsrcrecordid>eNotj0FKxDAYhYMoWEfBI2TpJmP-_GnTLGVQRxiYxczCXcmkCe0w05akIHXlEVx4Lg_hScygvMXH48GDj5Bb4HPgXNzvGzfOS6HOSAZaIstB4znJ0iQY5OL1klzFuE8VUKmM6M3UjY2LbaSmq6lt3LGNY5ho72nn3mgc2tD_fHx-f1GgicMUzHt_aDt3TS68OUR3888Z2T49bhdLtlo_vyweVswqoZgW1hvrfaFRaVNrI8DurJeICHlpOCiQrkjhJVpZSICd1EIrIXmhsC5xRu7-bm3oYwzOV0NojyZMFfDqZFydjKtkjL8Y_Era</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis and chemistry of new spiro‐Δ 1 ‐pyrazoline</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Louhichi, Nesrine ; Houas, Amel ; Hamadi, Naoufel Ben ; Msaddek, Moncef</creator><creatorcontrib>Louhichi, Nesrine ; Houas, Amel ; Hamadi, Naoufel Ben ; Msaddek, Moncef</creatorcontrib><description>In explorations of syntheses and chemistry of spiroheterocycles, we found that the reaction of 2‐diazopropane with (
E
)‐α‐arylidenepyrrolin‐2‐one, (
E
)‐α‐arylidene‐γ‐butyrolactone, and (
E
)‐arylidene‐
N
‐arylsuccinimide derivatives produced spiro‐Δ
1
‐pyrazolines. The photolysis of Δ
1
‐pyrazolines has led to cyclopropanes. The structures of the obtained adducts have been assigned by means of spectroscopic measurements. J. Heterocyclic Chem., (2011).</description><identifier>ISSN: 0022-152X</identifier><identifier>EISSN: 1943-5193</identifier><identifier>DOI: 10.1002/jhet.827</identifier><language>eng</language><ispartof>Journal of heterocyclic chemistry, 2012-03, Vol.49 (2), p.267-271</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c727-92cfacff69379ad9a21cbcf4333158a01714e6e6e083c46411b49297240673d83</citedby><cites>FETCH-LOGICAL-c727-92cfacff69379ad9a21cbcf4333158a01714e6e6e083c46411b49297240673d83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Louhichi, Nesrine</creatorcontrib><creatorcontrib>Houas, Amel</creatorcontrib><creatorcontrib>Hamadi, Naoufel Ben</creatorcontrib><creatorcontrib>Msaddek, Moncef</creatorcontrib><title>Synthesis and chemistry of new spiro‐Δ 1 ‐pyrazoline</title><title>Journal of heterocyclic chemistry</title><description>In explorations of syntheses and chemistry of spiroheterocycles, we found that the reaction of 2‐diazopropane with (
E
)‐α‐arylidenepyrrolin‐2‐one, (
E
)‐α‐arylidene‐γ‐butyrolactone, and (
E
)‐arylidene‐
N
‐arylsuccinimide derivatives produced spiro‐Δ
1
‐pyrazolines. The photolysis of Δ
1
‐pyrazolines has led to cyclopropanes. The structures of the obtained adducts have been assigned by means of spectroscopic measurements. J. Heterocyclic Chem., (2011).</description><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNotj0FKxDAYhYMoWEfBI2TpJmP-_GnTLGVQRxiYxczCXcmkCe0w05akIHXlEVx4Lg_hScygvMXH48GDj5Bb4HPgXNzvGzfOS6HOSAZaIstB4znJ0iQY5OL1klzFuE8VUKmM6M3UjY2LbaSmq6lt3LGNY5ho72nn3mgc2tD_fHx-f1GgicMUzHt_aDt3TS68OUR3888Z2T49bhdLtlo_vyweVswqoZgW1hvrfaFRaVNrI8DurJeICHlpOCiQrkjhJVpZSICd1EIrIXmhsC5xRu7-bm3oYwzOV0NojyZMFfDqZFydjKtkjL8Y_Era</recordid><startdate>201203</startdate><enddate>201203</enddate><creator>Louhichi, Nesrine</creator><creator>Houas, Amel</creator><creator>Hamadi, Naoufel Ben</creator><creator>Msaddek, Moncef</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201203</creationdate><title>Synthesis and chemistry of new spiro‐Δ 1 ‐pyrazoline</title><author>Louhichi, Nesrine ; Houas, Amel ; Hamadi, Naoufel Ben ; Msaddek, Moncef</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c727-92cfacff69379ad9a21cbcf4333158a01714e6e6e083c46411b49297240673d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Louhichi, Nesrine</creatorcontrib><creatorcontrib>Houas, Amel</creatorcontrib><creatorcontrib>Hamadi, Naoufel Ben</creatorcontrib><creatorcontrib>Msaddek, Moncef</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Louhichi, Nesrine</au><au>Houas, Amel</au><au>Hamadi, Naoufel Ben</au><au>Msaddek, Moncef</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and chemistry of new spiro‐Δ 1 ‐pyrazoline</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><date>2012-03</date><risdate>2012</risdate><volume>49</volume><issue>2</issue><spage>267</spage><epage>271</epage><pages>267-271</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>In explorations of syntheses and chemistry of spiroheterocycles, we found that the reaction of 2‐diazopropane with (
E
)‐α‐arylidenepyrrolin‐2‐one, (
E
)‐α‐arylidene‐γ‐butyrolactone, and (
E
)‐arylidene‐
N
‐arylsuccinimide derivatives produced spiro‐Δ
1
‐pyrazolines. The photolysis of Δ
1
‐pyrazolines has led to cyclopropanes. The structures of the obtained adducts have been assigned by means of spectroscopic measurements. J. Heterocyclic Chem., (2011).</abstract><doi>10.1002/jhet.827</doi><tpages>5</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0022-152X |
| ispartof | Journal of heterocyclic chemistry, 2012-03, Vol.49 (2), p.267-271 |
| issn | 0022-152X 1943-5193 |
| language | eng |
| recordid | cdi_crossref_primary_10_1002_jhet_827 |
| source | Wiley Online Library Journals Frontfile Complete |
| title | Synthesis and chemistry of new spiro‐Δ 1 ‐pyrazoline |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T19%3A47%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20chemistry%20of%20new%20spiro%E2%80%90%CE%94%201%20%E2%80%90pyrazoline&rft.jtitle=Journal%20of%20heterocyclic%20chemistry&rft.au=Louhichi,%20Nesrine&rft.date=2012-03&rft.volume=49&rft.issue=2&rft.spage=267&rft.epage=271&rft.pages=267-271&rft.issn=0022-152X&rft.eissn=1943-5193&rft_id=info:doi/10.1002/jhet.827&rft_dat=%3Ccrossref%3E10_1002_jhet_827%3C/crossref%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |