Synthesis of some novel S-alkylated and S-glycosylated hydantoin derivatives containing pyrene moiety
3-Aryl-5-[( Z )-pyrenylmethylene]-2-alkylthiohydantoins and 3-Aryl-5-[( Z )-pyrenylmethylene]-2-( D -glycosyl)-2-thiohydantoins functionalized with different aromatic and glycoside substituents have been synthesized by the reaction of ( Z )-3-(4-methoxyphenyl)-5-[(pyren-8-yl)methylene]-2-thiohydanto...
Gespeichert in:
| Veröffentlicht in: | Russian journal of general chemistry 2016-04, Vol.86 (4), p.919-923 |
|---|---|
| Hauptverfasser: | , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 923 |
|---|---|
| container_issue | 4 |
| container_start_page | 919 |
| container_title | Russian journal of general chemistry |
| container_volume | 86 |
| creator | Khalifa, N. M. Nossier, E. S. Al-Omar, M. A. Amr, A. E. |
| description | 3-Aryl-5-[(
Z
)-pyrenylmethylene]-2-alkylthiohydantoins and 3-Aryl-5-[(
Z
)-pyrenylmethylene]-2-(
D
-glycosyl)-2-thiohydantoins functionalized with different aromatic and glycoside substituents have been synthesized by the reaction of (
Z
)-3-(4-methoxyphenyl)-5-[(pyren-8-yl)methylene]-2-thiohydantoin with alkyl halides, cyclic and acyclic nucleosides via various routes with moderate to good yields and characterized by
1
H,
13
C NMR and mass spectra and elemental analysis |
| doi_str_mv | 10.1134/S1070363216040277 |
| format | Article |
| fullrecord | <record><control><sourceid>crossref_sprin</sourceid><recordid>TN_cdi_crossref_primary_10_1134_S1070363216040277</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1134_S1070363216040277</sourcerecordid><originalsourceid>FETCH-LOGICAL-c288t-2b2b38ef8d7b90cfdfba5e21907f9909ca40ff2821fae6ee8f95cd845426a7453</originalsourceid><addsrcrecordid>eNp9kN1KAzEQhYMoWKsP4F1eYHWS7E_2Uop_UPCier1kN5M2dZuUJBby9m5p7wSv5syc-YbhEHLP4IExUT6uGDQgasFZDSXwprkgs0nKQogKLic92cXRvyY3MW4BGEDNZwRX2aUNRhupNzT6HVLnDzjSVaHG7zyqhJoqp6d-PebBx_Nok7VyyVtHNQZ7UMkeMNLBu6Sss25N9zmgQ7rzFlO-JVdGjRHvznVOvl6ePxdvxfLj9X3xtCwGLmUqeM97IdFI3fQtDEabXlXIWQuNaVtoB1WCMVxyZhTWiNK01aBlWZW8Vk1ZiTlhp7tD8DEGNN0-2J0KuWPQHXPq_uQ0MfzExGnXrTF0W_8T3PTmP9Av33lslA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis of some novel S-alkylated and S-glycosylated hydantoin derivatives containing pyrene moiety</title><source>SpringerLink Journals - AutoHoldings</source><creator>Khalifa, N. M. ; Nossier, E. S. ; Al-Omar, M. A. ; Amr, A. E.</creator><creatorcontrib>Khalifa, N. M. ; Nossier, E. S. ; Al-Omar, M. A. ; Amr, A. E.</creatorcontrib><description>3-Aryl-5-[(
Z
)-pyrenylmethylene]-2-alkylthiohydantoins and 3-Aryl-5-[(
Z
)-pyrenylmethylene]-2-(
D
-glycosyl)-2-thiohydantoins functionalized with different aromatic and glycoside substituents have been synthesized by the reaction of (
Z
)-3-(4-methoxyphenyl)-5-[(pyren-8-yl)methylene]-2-thiohydantoin with alkyl halides, cyclic and acyclic nucleosides via various routes with moderate to good yields and characterized by
1
H,
13
C NMR and mass spectra and elemental analysis</description><identifier>ISSN: 1070-3632</identifier><identifier>EISSN: 1608-3350</identifier><identifier>DOI: 10.1134/S1070363216040277</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science</subject><ispartof>Russian journal of general chemistry, 2016-04, Vol.86 (4), p.919-923</ispartof><rights>Pleiades Publishing, Ltd. 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c288t-2b2b38ef8d7b90cfdfba5e21907f9909ca40ff2821fae6ee8f95cd845426a7453</citedby><cites>FETCH-LOGICAL-c288t-2b2b38ef8d7b90cfdfba5e21907f9909ca40ff2821fae6ee8f95cd845426a7453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1070363216040277$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1070363216040277$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids></links><search><creatorcontrib>Khalifa, N. M.</creatorcontrib><creatorcontrib>Nossier, E. S.</creatorcontrib><creatorcontrib>Al-Omar, M. A.</creatorcontrib><creatorcontrib>Amr, A. E.</creatorcontrib><title>Synthesis of some novel S-alkylated and S-glycosylated hydantoin derivatives containing pyrene moiety</title><title>Russian journal of general chemistry</title><addtitle>Russ J Gen Chem</addtitle><description>3-Aryl-5-[(
Z
)-pyrenylmethylene]-2-alkylthiohydantoins and 3-Aryl-5-[(
Z
)-pyrenylmethylene]-2-(
D
-glycosyl)-2-thiohydantoins functionalized with different aromatic and glycoside substituents have been synthesized by the reaction of (
Z
)-3-(4-methoxyphenyl)-5-[(pyren-8-yl)methylene]-2-thiohydantoin with alkyl halides, cyclic and acyclic nucleosides via various routes with moderate to good yields and characterized by
1
H,
13
C NMR and mass spectra and elemental analysis</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kN1KAzEQhYMoWKsP4F1eYHWS7E_2Uop_UPCier1kN5M2dZuUJBby9m5p7wSv5syc-YbhEHLP4IExUT6uGDQgasFZDSXwprkgs0nKQogKLic92cXRvyY3MW4BGEDNZwRX2aUNRhupNzT6HVLnDzjSVaHG7zyqhJoqp6d-PebBx_Nok7VyyVtHNQZ7UMkeMNLBu6Sss25N9zmgQ7rzFlO-JVdGjRHvznVOvl6ePxdvxfLj9X3xtCwGLmUqeM97IdFI3fQtDEabXlXIWQuNaVtoB1WCMVxyZhTWiNK01aBlWZW8Vk1ZiTlhp7tD8DEGNN0-2J0KuWPQHXPq_uQ0MfzExGnXrTF0W_8T3PTmP9Av33lslA</recordid><startdate>20160401</startdate><enddate>20160401</enddate><creator>Khalifa, N. M.</creator><creator>Nossier, E. S.</creator><creator>Al-Omar, M. A.</creator><creator>Amr, A. E.</creator><general>Pleiades Publishing</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20160401</creationdate><title>Synthesis of some novel S-alkylated and S-glycosylated hydantoin derivatives containing pyrene moiety</title><author>Khalifa, N. M. ; Nossier, E. S. ; Al-Omar, M. A. ; Amr, A. E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c288t-2b2b38ef8d7b90cfdfba5e21907f9909ca40ff2821fae6ee8f95cd845426a7453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khalifa, N. M.</creatorcontrib><creatorcontrib>Nossier, E. S.</creatorcontrib><creatorcontrib>Al-Omar, M. A.</creatorcontrib><creatorcontrib>Amr, A. E.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khalifa, N. M.</au><au>Nossier, E. S.</au><au>Al-Omar, M. A.</au><au>Amr, A. E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of some novel S-alkylated and S-glycosylated hydantoin derivatives containing pyrene moiety</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2016-04-01</date><risdate>2016</risdate><volume>86</volume><issue>4</issue><spage>919</spage><epage>923</epage><pages>919-923</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>3-Aryl-5-[(
Z
)-pyrenylmethylene]-2-alkylthiohydantoins and 3-Aryl-5-[(
Z
)-pyrenylmethylene]-2-(
D
-glycosyl)-2-thiohydantoins functionalized with different aromatic and glycoside substituents have been synthesized by the reaction of (
Z
)-3-(4-methoxyphenyl)-5-[(pyren-8-yl)methylene]-2-thiohydantoin with alkyl halides, cyclic and acyclic nucleosides via various routes with moderate to good yields and characterized by
1
H,
13
C NMR and mass spectra and elemental analysis</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070363216040277</doi><tpages>5</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1070-3632 |
| ispartof | Russian journal of general chemistry, 2016-04, Vol.86 (4), p.919-923 |
| issn | 1070-3632 1608-3350 |
| language | eng |
| recordid | cdi_crossref_primary_10_1134_S1070363216040277 |
| source | SpringerLink Journals - AutoHoldings |
| subjects | Chemistry Chemistry and Materials Science Chemistry/Food Science |
| title | Synthesis of some novel S-alkylated and S-glycosylated hydantoin derivatives containing pyrene moiety |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T17%3A55%3A49IST&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%20some%20novel%20S-alkylated%20and%20S-glycosylated%20hydantoin%20derivatives%20containing%20pyrene%20moiety&rft.jtitle=Russian%20journal%20of%20general%20chemistry&rft.au=Khalifa,%20N.%20M.&rft.date=2016-04-01&rft.volume=86&rft.issue=4&rft.spage=919&rft.epage=923&rft.pages=919-923&rft.issn=1070-3632&rft.eissn=1608-3350&rft_id=info:doi/10.1134/S1070363216040277&rft_dat=%3Ccrossref_sprin%3E10_1134_S1070363216040277%3C/crossref_sprin%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 |