Synthesis of new spirobenzopyrans with two long-chain substituents
Two new photochromic compounds each containing two substituents with long alkyl chains in different parts of a molecule were synthesized by a sequence of direct reduction, acylation, and nitration reactions of substituted spirobenzopyrans. The structures of the compounds synthesized were determined...
Gespeichert in:
Veröffentlicht in: | Russian chemical bulletin 2005-11, Vol.54 (11), p.2612-2615 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2615 |
---|---|
container_issue | 11 |
container_start_page | 2612 |
container_title | Russian chemical bulletin |
container_volume | 54 |
creator | Zaichenko, N. L. Kol’tsova, L. S. Shiyonok, A. I. Venidiktova, O. V. Barachevsky, V. A. Marevtsev, V. S. |
description | Two new photochromic compounds each containing two substituents with long alkyl chains in different parts of a molecule were synthesized by a sequence of direct reduction, acylation, and nitration reactions of substituted spirobenzopyrans. The structures of the compounds synthesized were determined using the 1H NMR spectra. |
doi_str_mv | 10.1007/s11172-006-0164-8 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2664471586</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2664471586</sourcerecordid><originalsourceid>FETCH-LOGICAL-c273t-425bf655f1bd016e8ebbc8fa976f2ada6c2b4e6629a9af936e336c344447bc4b3</originalsourceid><addsrcrecordid>eNotkMtKAzEUhoMoWKsP4C7gOprL5DJLLd6g4EJdhyRN7JSajEmGUp_elHo25yw-zv_zAXBN8C3BWN4VQoikCGOBMBEdUidgRrhkqCeSnLYbC4E4VfwcXJSywRhTpdQMPLzvY137MhSYAox-B8s45GR9_E3jPptY4G6oa1h3CW5T_EJubYYIy2RLHerkYy2X4CyYbfFX_3sOPp8ePxYvaPn2_Lq4XyJHJauoo9wGwXkgdtUqeuWtdSqYXopAzcoIR23nhaC96U3omfCMCce6NtK6zrI5uDn-HXP6mXypepOmHFukpkI0inAlGkWOlMuplOyDHvPwbfJeE6wPqvRRlW6q9EGVVuwPSmhdGQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2664471586</pqid></control><display><type>article</type><title>Synthesis of new spirobenzopyrans with two long-chain substituents</title><source>SpringerLink Journals - AutoHoldings</source><creator>Zaichenko, N. L. ; Kol’tsova, L. S. ; Shiyonok, A. I. ; Venidiktova, O. V. ; Barachevsky, V. A. ; Marevtsev, V. S.</creator><creatorcontrib>Zaichenko, N. L. ; Kol’tsova, L. S. ; Shiyonok, A. I. ; Venidiktova, O. V. ; Barachevsky, V. A. ; Marevtsev, V. S.</creatorcontrib><description>Two new photochromic compounds each containing two substituents with long alkyl chains in different parts of a molecule were synthesized by a sequence of direct reduction, acylation, and nitration reactions of substituted spirobenzopyrans. The structures of the compounds synthesized were determined using the 1H NMR spectra.</description><identifier>ISSN: 1066-5285</identifier><identifier>EISSN: 1573-9171</identifier><identifier>DOI: 10.1007/s11172-006-0164-8</identifier><language>eng</language><publisher>New York: Springer Nature B.V</publisher><subject>Acylation ; Chemical synthesis ; Direct reduction ; Nitration ; NMR ; Nuclear magnetic resonance</subject><ispartof>Russian chemical bulletin, 2005-11, Vol.54 (11), p.2612-2615</ispartof><rights>Springer Science+Business Media, Inc. 2005.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c273t-425bf655f1bd016e8ebbc8fa976f2ada6c2b4e6629a9af936e336c344447bc4b3</citedby><cites>FETCH-LOGICAL-c273t-425bf655f1bd016e8ebbc8fa976f2ada6c2b4e6629a9af936e336c344447bc4b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids></links><search><creatorcontrib>Zaichenko, N. L.</creatorcontrib><creatorcontrib>Kol’tsova, L. S.</creatorcontrib><creatorcontrib>Shiyonok, A. I.</creatorcontrib><creatorcontrib>Venidiktova, O. V.</creatorcontrib><creatorcontrib>Barachevsky, V. A.</creatorcontrib><creatorcontrib>Marevtsev, V. S.</creatorcontrib><title>Synthesis of new spirobenzopyrans with two long-chain substituents</title><title>Russian chemical bulletin</title><description>Two new photochromic compounds each containing two substituents with long alkyl chains in different parts of a molecule were synthesized by a sequence of direct reduction, acylation, and nitration reactions of substituted spirobenzopyrans. The structures of the compounds synthesized were determined using the 1H NMR spectra.</description><subject>Acylation</subject><subject>Chemical synthesis</subject><subject>Direct reduction</subject><subject>Nitration</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><issn>1066-5285</issn><issn>1573-9171</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNotkMtKAzEUhoMoWKsP4C7gOprL5DJLLd6g4EJdhyRN7JSajEmGUp_elHo25yw-zv_zAXBN8C3BWN4VQoikCGOBMBEdUidgRrhkqCeSnLYbC4E4VfwcXJSywRhTpdQMPLzvY137MhSYAox-B8s45GR9_E3jPptY4G6oa1h3CW5T_EJubYYIy2RLHerkYy2X4CyYbfFX_3sOPp8ePxYvaPn2_Lq4XyJHJauoo9wGwXkgdtUqeuWtdSqYXopAzcoIR23nhaC96U3omfCMCce6NtK6zrI5uDn-HXP6mXypepOmHFukpkI0inAlGkWOlMuplOyDHvPwbfJeE6wPqvRRlW6q9EGVVuwPSmhdGQ</recordid><startdate>20051101</startdate><enddate>20051101</enddate><creator>Zaichenko, N. L.</creator><creator>Kol’tsova, L. S.</creator><creator>Shiyonok, A. I.</creator><creator>Venidiktova, O. V.</creator><creator>Barachevsky, V. A.</creator><creator>Marevtsev, V. S.</creator><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20051101</creationdate><title>Synthesis of new spirobenzopyrans with two long-chain substituents</title><author>Zaichenko, N. L. ; Kol’tsova, L. S. ; Shiyonok, A. I. ; Venidiktova, O. V. ; Barachevsky, V. A. ; Marevtsev, V. S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c273t-425bf655f1bd016e8ebbc8fa976f2ada6c2b4e6629a9af936e336c344447bc4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Acylation</topic><topic>Chemical synthesis</topic><topic>Direct reduction</topic><topic>Nitration</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zaichenko, N. L.</creatorcontrib><creatorcontrib>Kol’tsova, L. S.</creatorcontrib><creatorcontrib>Shiyonok, A. I.</creatorcontrib><creatorcontrib>Venidiktova, O. V.</creatorcontrib><creatorcontrib>Barachevsky, V. A.</creatorcontrib><creatorcontrib>Marevtsev, V. S.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian chemical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zaichenko, N. L.</au><au>Kol’tsova, L. S.</au><au>Shiyonok, A. I.</au><au>Venidiktova, O. V.</au><au>Barachevsky, V. A.</au><au>Marevtsev, V. S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of new spirobenzopyrans with two long-chain substituents</atitle><jtitle>Russian chemical bulletin</jtitle><date>2005-11-01</date><risdate>2005</risdate><volume>54</volume><issue>11</issue><spage>2612</spage><epage>2615</epage><pages>2612-2615</pages><issn>1066-5285</issn><eissn>1573-9171</eissn><abstract>Two new photochromic compounds each containing two substituents with long alkyl chains in different parts of a molecule were synthesized by a sequence of direct reduction, acylation, and nitration reactions of substituted spirobenzopyrans. The structures of the compounds synthesized were determined using the 1H NMR spectra.</abstract><cop>New York</cop><pub>Springer Nature B.V</pub><doi>10.1007/s11172-006-0164-8</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1066-5285 |
ispartof | Russian chemical bulletin, 2005-11, Vol.54 (11), p.2612-2615 |
issn | 1066-5285 1573-9171 |
language | eng |
recordid | cdi_proquest_journals_2664471586 |
source | SpringerLink Journals - AutoHoldings |
subjects | Acylation Chemical synthesis Direct reduction Nitration NMR Nuclear magnetic resonance |
title | Synthesis of new spirobenzopyrans with two long-chain substituents |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T00%3A34%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20new%20spirobenzopyrans%20with%20two%20long-chain%20substituents&rft.jtitle=Russian%20chemical%20bulletin&rft.au=Zaichenko,%20N.%20L.&rft.date=2005-11-01&rft.volume=54&rft.issue=11&rft.spage=2612&rft.epage=2615&rft.pages=2612-2615&rft.issn=1066-5285&rft.eissn=1573-9171&rft_id=info:doi/10.1007/s11172-006-0164-8&rft_dat=%3Cproquest_cross%3E2664471586%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2664471586&rft_id=info:pmid/&rfr_iscdi=true |