Novel oxidative ring opening reaction of H-isotelluro-chromenes to bis(o-formylstyryl) ditellurides
The oxidation of 1-unsubstituted or 1-phenyl-1H-isotellurochromenes with m-chloroperbenzoic acid (mCPBA) in CHCl3 resulted in a ring opening reaction to produce as the sole products the corresponding o-formyl or benzoyl distyryl ditellurides, which were also produced by the hydrolysis of the 2-benzo...
Gespeichert in:
| Veröffentlicht in: | Molecules (Basel, Switzerland) Switzerland), 2010-03, Vol.15 (3), p.1466-1472 |
|---|---|
| Hauptverfasser: | , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 1472 |
|---|---|
| container_issue | 3 |
| container_start_page | 1466 |
| container_title | Molecules (Basel, Switzerland) |
| container_volume | 15 |
| creator | Sashida, Haruki Satoh, Hirohito Ohyanagi, Kazuo Kaname, Mamoru |
| description | The oxidation of 1-unsubstituted or 1-phenyl-1H-isotellurochromenes with m-chloroperbenzoic acid (mCPBA) in CHCl3 resulted in a ring opening reaction to produce as the sole products the corresponding o-formyl or benzoyl distyryl ditellurides, which were also produced by the hydrolysis of the 2-benzotelluropyrylium salts readily prepared from the parent isotellurochromene. |
| doi_str_mv | 10.3390/molecules15031466 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_733810438</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>733810438</sourcerecordid><originalsourceid>FETCH-LOGICAL-p554-6352d05729ae1d1123940bbe7e3fc303f16462e67f947c95b81a107ddcc875d53</originalsourceid><addsrcrecordid>eNo1kLFOwzAURS0kREvhA1iQN2Aw2Hl2Eo-oAopUwdI9SuwXMHLiYicV-XuKWqazHF0dXUKuBL8H0PyhCx7N6DEJxUHIPD8hcyEzzoBLPSPnKX1xngkp1BmZZRxAaS3nxLyFHXoafpytB7dDGl3_QcMW-z9GrM3gQk9DS1fMpTCg92MMzHzG0GGPiQ6BNi7dBtaG2E0-DVOc_B217qA6i-mCnLa1T3h55IJsnp82yxVbv7-8Lh_XbKuUZDmozHJVZLpGYYXIQEveNFggtAY4tCKXeYZ50WpZGK2aUtSCF9YaUxbKKliQm8PsNobvEdNQdS6ZfUXdYxhTVQCUgkso9-b10RybDm21ja6r41T93wK_F4Vlpw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>733810438</pqid></control><display><type>article</type><title>Novel oxidative ring opening reaction of H-isotelluro-chromenes to bis(o-formylstyryl) ditellurides</title><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Sashida, Haruki ; Satoh, Hirohito ; Ohyanagi, Kazuo ; Kaname, Mamoru</creator><creatorcontrib>Sashida, Haruki ; Satoh, Hirohito ; Ohyanagi, Kazuo ; Kaname, Mamoru</creatorcontrib><description>The oxidation of 1-unsubstituted or 1-phenyl-1H-isotellurochromenes with m-chloroperbenzoic acid (mCPBA) in CHCl3 resulted in a ring opening reaction to produce as the sole products the corresponding o-formyl or benzoyl distyryl ditellurides, which were also produced by the hydrolysis of the 2-benzotelluropyrylium salts readily prepared from the parent isotellurochromene.</description><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules15031466</identifier><identifier>PMID: 20335994</identifier><language>eng</language><publisher>Switzerland</publisher><subject>Benzopyrans - chemistry ; Magnetic Resonance Spectroscopy ; Mass Spectrometry ; Spectrophotometry, Infrared ; Tellurium - chemistry</subject><ispartof>Molecules (Basel, Switzerland), 2010-03, Vol.15 (3), p.1466-1472</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20335994$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sashida, Haruki</creatorcontrib><creatorcontrib>Satoh, Hirohito</creatorcontrib><creatorcontrib>Ohyanagi, Kazuo</creatorcontrib><creatorcontrib>Kaname, Mamoru</creatorcontrib><title>Novel oxidative ring opening reaction of H-isotelluro-chromenes to bis(o-formylstyryl) ditellurides</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>The oxidation of 1-unsubstituted or 1-phenyl-1H-isotellurochromenes with m-chloroperbenzoic acid (mCPBA) in CHCl3 resulted in a ring opening reaction to produce as the sole products the corresponding o-formyl or benzoyl distyryl ditellurides, which were also produced by the hydrolysis of the 2-benzotelluropyrylium salts readily prepared from the parent isotellurochromene.</description><subject>Benzopyrans - chemistry</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Mass Spectrometry</subject><subject>Spectrophotometry, Infrared</subject><subject>Tellurium - chemistry</subject><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kLFOwzAURS0kREvhA1iQN2Aw2Hl2Eo-oAopUwdI9SuwXMHLiYicV-XuKWqazHF0dXUKuBL8H0PyhCx7N6DEJxUHIPD8hcyEzzoBLPSPnKX1xngkp1BmZZRxAaS3nxLyFHXoafpytB7dDGl3_QcMW-z9GrM3gQk9DS1fMpTCg92MMzHzG0GGPiQ6BNi7dBtaG2E0-DVOc_B217qA6i-mCnLa1T3h55IJsnp82yxVbv7-8Lh_XbKuUZDmozHJVZLpGYYXIQEveNFggtAY4tCKXeYZ50WpZGK2aUtSCF9YaUxbKKliQm8PsNobvEdNQdS6ZfUXdYxhTVQCUgkso9-b10RybDm21ja6r41T93wK_F4Vlpw</recordid><startdate>20100309</startdate><enddate>20100309</enddate><creator>Sashida, Haruki</creator><creator>Satoh, Hirohito</creator><creator>Ohyanagi, Kazuo</creator><creator>Kaname, Mamoru</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20100309</creationdate><title>Novel oxidative ring opening reaction of H-isotelluro-chromenes to bis(o-formylstyryl) ditellurides</title><author>Sashida, Haruki ; Satoh, Hirohito ; Ohyanagi, Kazuo ; Kaname, Mamoru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p554-6352d05729ae1d1123940bbe7e3fc303f16462e67f947c95b81a107ddcc875d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Benzopyrans - chemistry</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Mass Spectrometry</topic><topic>Spectrophotometry, Infrared</topic><topic>Tellurium - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sashida, Haruki</creatorcontrib><creatorcontrib>Satoh, Hirohito</creatorcontrib><creatorcontrib>Ohyanagi, Kazuo</creatorcontrib><creatorcontrib>Kaname, Mamoru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sashida, Haruki</au><au>Satoh, Hirohito</au><au>Ohyanagi, Kazuo</au><au>Kaname, Mamoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel oxidative ring opening reaction of H-isotelluro-chromenes to bis(o-formylstyryl) ditellurides</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2010-03-09</date><risdate>2010</risdate><volume>15</volume><issue>3</issue><spage>1466</spage><epage>1472</epage><pages>1466-1472</pages><eissn>1420-3049</eissn><abstract>The oxidation of 1-unsubstituted or 1-phenyl-1H-isotellurochromenes with m-chloroperbenzoic acid (mCPBA) in CHCl3 resulted in a ring opening reaction to produce as the sole products the corresponding o-formyl or benzoyl distyryl ditellurides, which were also produced by the hydrolysis of the 2-benzotelluropyrylium salts readily prepared from the parent isotellurochromene.</abstract><cop>Switzerland</cop><pmid>20335994</pmid><doi>10.3390/molecules15031466</doi><tpages>7</tpages></addata></record> |
| fulltext | fulltext |
| identifier | EISSN: 1420-3049 |
| ispartof | Molecules (Basel, Switzerland), 2010-03, Vol.15 (3), p.1466-1472 |
| issn | 1420-3049 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_733810438 |
| source | MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry |
| subjects | Benzopyrans - chemistry Magnetic Resonance Spectroscopy Mass Spectrometry Spectrophotometry, Infrared Tellurium - chemistry |
| title | Novel oxidative ring opening reaction of H-isotelluro-chromenes to bis(o-formylstyryl) ditellurides |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-15T09%3A10%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Novel%20oxidative%20ring%20opening%20reaction%20of%20H-isotelluro-chromenes%20to%20bis(o-formylstyryl)%20ditellurides&rft.jtitle=Molecules%20(Basel,%20Switzerland)&rft.au=Sashida,%20Haruki&rft.date=2010-03-09&rft.volume=15&rft.issue=3&rft.spage=1466&rft.epage=1472&rft.pages=1466-1472&rft.eissn=1420-3049&rft_id=info:doi/10.3390/molecules15031466&rft_dat=%3Cproquest_pubme%3E733810438%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=733810438&rft_id=info:pmid/20335994&rfr_iscdi=true |