Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles
New hybrid compounds of abietic acid with 2-thione-, 2-alkylthio-, and 2-alkylamino-1,3,4-oxadiazole fragments at various distances from the diterpene skeleton were synthesized in situ via cyclization in acidic medium of intermediate dithiocarbamates or cyclodesulfurization of intermediate acylthios...
Gespeichert in:
| Veröffentlicht in: | Chemistry of natural compounds 2022-03, Vol.58 (2), p.290-296 |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 296 |
|---|---|
| container_issue | 2 |
| container_start_page | 290 |
| container_title | Chemistry of natural compounds |
| container_volume | 58 |
| creator | Shpatov, A. V. Zakharova, S. S. Popov, S. A. |
| description | New hybrid compounds of abietic acid with 2-thione-, 2-alkylthio-, and 2-alkylamino-1,3,4-oxadiazole fragments at various distances from the diterpene skeleton were synthesized in situ via cyclization in acidic medium of intermediate dithiocarbamates or cyclodesulfurization of intermediate acylthiosemicarbazides through the action of Hg(OAc)
2
. |
| doi_str_mv | 10.1007/s10600-022-03662-5 |
| format | Article |
| fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_2665621587</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A704165333</galeid><sourcerecordid>A704165333</sourcerecordid><originalsourceid>FETCH-LOGICAL-c309t-4598a222f1d8aaaee6c7a3d6e5039c540dd47f3d77accb7c84b37375368e80c83</originalsourceid><addsrcrecordid>eNp9kE1LAzEQhoMoWKt_wNOC16ZOks1HL0IpaoViD-o5ZJNsTWl3a7Ki9dcbu4I3Zw7DDO8zM7wIXRIYEwB5nQgIAAyUYmBCUMyP0IBwybBiSh2jAQBMMCMMTtFZSuvcKiHUAN087Zvu1aeQirYuHv1HMd9XMbhDO62C74Itpja4wjSuICM2KvHy07hgvtqNT-fopDab5C9-6xC93N0-z-Z4sbx_mE0X2DKYdLjkE2UopTVxyhjjvbDSMCc8BzaxvATnSlkzJ6WxtpJWlRWTTHImlFdgFRuiq37vLrZv7z51et2-xyaf1FQILijhSmbVuFetzMbr0NRtF43N6fw22LbxdcjzqYSSCM5yDBHtARvblKKv9S6GrYl7TUD_GKt7Y3U2Vh-M1TxDrIdSFjcrH_9--Yf6BgcueDI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2665621587</pqid></control><display><type>article</type><title>Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles</title><source>Springer Nature - Complete Springer Journals</source><creator>Shpatov, A. V. ; Zakharova, S. S. ; Popov, S. A.</creator><creatorcontrib>Shpatov, A. V. ; Zakharova, S. S. ; Popov, S. A.</creatorcontrib><description>New hybrid compounds of abietic acid with 2-thione-, 2-alkylthio-, and 2-alkylamino-1,3,4-oxadiazole fragments at various distances from the diterpene skeleton were synthesized in situ via cyclization in acidic medium of intermediate dithiocarbamates or cyclodesulfurization of intermediate acylthiosemicarbazides through the action of Hg(OAc)
2
.</description><identifier>ISSN: 0009-3130</identifier><identifier>EISSN: 1573-8388</identifier><identifier>DOI: 10.1007/s10600-022-03662-5</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Organic Chemistry ; Oxadiazoles ; Plant Sciences</subject><ispartof>Chemistry of natural compounds, 2022-03, Vol.58 (2), p.290-296</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2022</rights><rights>COPYRIGHT 2022 Springer</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c309t-4598a222f1d8aaaee6c7a3d6e5039c540dd47f3d77accb7c84b37375368e80c83</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/s10600-022-03662-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10600-022-03662-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Shpatov, A. V.</creatorcontrib><creatorcontrib>Zakharova, S. S.</creatorcontrib><creatorcontrib>Popov, S. A.</creatorcontrib><title>Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles</title><title>Chemistry of natural compounds</title><addtitle>Chem Nat Compd</addtitle><description>New hybrid compounds of abietic acid with 2-thione-, 2-alkylthio-, and 2-alkylamino-1,3,4-oxadiazole fragments at various distances from the diterpene skeleton were synthesized in situ via cyclization in acidic medium of intermediate dithiocarbamates or cyclodesulfurization of intermediate acylthiosemicarbazides through the action of Hg(OAc)
2
.</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Organic Chemistry</subject><subject>Oxadiazoles</subject><subject>Plant Sciences</subject><issn>0009-3130</issn><issn>1573-8388</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMoWKt_wNOC16ZOks1HL0IpaoViD-o5ZJNsTWl3a7Ki9dcbu4I3Zw7DDO8zM7wIXRIYEwB5nQgIAAyUYmBCUMyP0IBwybBiSh2jAQBMMCMMTtFZSuvcKiHUAN087Zvu1aeQirYuHv1HMd9XMbhDO62C74Itpja4wjSuICM2KvHy07hgvtqNT-fopDab5C9-6xC93N0-z-Z4sbx_mE0X2DKYdLjkE2UopTVxyhjjvbDSMCc8BzaxvATnSlkzJ6WxtpJWlRWTTHImlFdgFRuiq37vLrZv7z51et2-xyaf1FQILijhSmbVuFetzMbr0NRtF43N6fw22LbxdcjzqYSSCM5yDBHtARvblKKv9S6GrYl7TUD_GKt7Y3U2Vh-M1TxDrIdSFjcrH_9--Yf6BgcueDI</recordid><startdate>20220301</startdate><enddate>20220301</enddate><creator>Shpatov, A. V.</creator><creator>Zakharova, S. S.</creator><creator>Popov, S. A.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20220301</creationdate><title>Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles</title><author>Shpatov, A. V. ; Zakharova, S. S. ; Popov, S. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c309t-4598a222f1d8aaaee6c7a3d6e5039c540dd47f3d77accb7c84b37375368e80c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Organic Chemistry</topic><topic>Oxadiazoles</topic><topic>Plant Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shpatov, A. V.</creatorcontrib><creatorcontrib>Zakharova, S. S.</creatorcontrib><creatorcontrib>Popov, S. A.</creatorcontrib><collection>CrossRef</collection><jtitle>Chemistry of natural compounds</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shpatov, A. V.</au><au>Zakharova, S. S.</au><au>Popov, S. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles</atitle><jtitle>Chemistry of natural compounds</jtitle><stitle>Chem Nat Compd</stitle><date>2022-03-01</date><risdate>2022</risdate><volume>58</volume><issue>2</issue><spage>290</spage><epage>296</epage><pages>290-296</pages><issn>0009-3130</issn><eissn>1573-8388</eissn><abstract>New hybrid compounds of abietic acid with 2-thione-, 2-alkylthio-, and 2-alkylamino-1,3,4-oxadiazole fragments at various distances from the diterpene skeleton were synthesized in situ via cyclization in acidic medium of intermediate dithiocarbamates or cyclodesulfurization of intermediate acylthiosemicarbazides through the action of Hg(OAc)
2
.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10600-022-03662-5</doi><tpages>7</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0009-3130 |
| ispartof | Chemistry of natural compounds, 2022-03, Vol.58 (2), p.290-296 |
| issn | 0009-3130 1573-8388 |
| language | eng |
| recordid | cdi_proquest_journals_2665621587 |
| source | Springer Nature - Complete Springer Journals |
| subjects | Chemistry Chemistry and Materials Science Chemistry/Food Science Organic Chemistry Oxadiazoles Plant Sciences |
| title | Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T22%3A15%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20New%20Hybrids%20of%20Abietic%20Acid%20and%201,3,4-Oxadiazoles&rft.jtitle=Chemistry%20of%20natural%20compounds&rft.au=Shpatov,%20A.%20V.&rft.date=2022-03-01&rft.volume=58&rft.issue=2&rft.spage=290&rft.epage=296&rft.pages=290-296&rft.issn=0009-3130&rft.eissn=1573-8388&rft_id=info:doi/10.1007/s10600-022-03662-5&rft_dat=%3Cgale_proqu%3EA704165333%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2665621587&rft_id=info:pmid/&rft_galeid=A704165333&rfr_iscdi=true |