Formation of a Tetrahydrofuran Derivative from Diallyl
WHEN diallyl (hexa-1: 5-diene) is treated with perbenzoic acid, 1: 2-5: 6-diepoxyhexane (I) is produced in good yield (80 per cent).
Gespeichert in:
Veröffentlicht in: | Nature (London) 1949-09, Vol.164 (4166), p.402-403 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 403 |
---|---|
container_issue | 4166 |
container_start_page | 402 |
container_title | Nature (London) |
container_volume | 164 |
creator | WOOD, D. J. C WIGGINS, L. F |
description | WHEN diallyl (hexa-1: 5-diene) is treated with perbenzoic acid, 1: 2-5: 6-diepoxyhexane (I) is produced in good yield (80 per cent). |
doi_str_mv | 10.1038/164402b0 |
format | Article |
fullrecord | <record><control><sourceid>nature_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1038_164402b0</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>164402b0</sourcerecordid><originalsourceid>FETCH-LOGICAL-c284t-b4852936129f9662a8ee214967ccf720ee6e26e530155cd1a81b3c2310c5173</originalsourceid><addsrcrecordid>eNptz09Lw0AQBfBFFIxV8BNIjnqIzv7JZnOU1qpQ8GDvYbOd1ZQkK5OkkG9vJBYvnuYwPx7vMXbN4Z6DNA9cKwWihBMWcZXpRGmTnbIIQJgEjNTn7KLr9gCQ8kxFTK8DNbavQhsHH9t4iz3Zz3FHwQ9k23iFVB2m_wFjT6GJV5Wt67G-ZGfe1h1e_d4Fe18_bZcvyebt-XX5uEmcMKpPSmVSkUvNRe5zrYU1iIKrXGfO-UwAokahMZXA09TtuDW8lE5IDm6qJxfsdk51FLqO0BdfVDWWxoJD8bO2OK6d6N1Mu4m0H0jFPgzUTt3-szezbW0_EP6FHsE3_NJc0w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Formation of a Tetrahydrofuran Derivative from Diallyl</title><source>Nature</source><source>SpringerLink Journals - AutoHoldings</source><creator>WOOD, D. J. C ; WIGGINS, L. F</creator><creatorcontrib>WOOD, D. J. C ; WIGGINS, L. F</creatorcontrib><description>WHEN diallyl (hexa-1: 5-diene) is treated with perbenzoic acid, 1: 2-5: 6-diepoxyhexane (I) is produced in good yield (80 per cent).</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/164402b0</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Humanities and Social Sciences ; letter ; multidisciplinary ; Science ; Science (multidisciplinary)</subject><ispartof>Nature (London), 1949-09, Vol.164 (4166), p.402-403</ispartof><rights>Springer Nature Limited 1949</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c284t-b4852936129f9662a8ee214967ccf720ee6e26e530155cd1a81b3c2310c5173</citedby><cites>FETCH-LOGICAL-c284t-b4852936129f9662a8ee214967ccf720ee6e26e530155cd1a81b3c2310c5173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/164402b0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/164402b0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,2725,27923,27924,41487,42556,51318</link.rule.ids></links><search><creatorcontrib>WOOD, D. J. C</creatorcontrib><creatorcontrib>WIGGINS, L. F</creatorcontrib><title>Formation of a Tetrahydrofuran Derivative from Diallyl</title><title>Nature (London)</title><addtitle>Nature</addtitle><description>WHEN diallyl (hexa-1: 5-diene) is treated with perbenzoic acid, 1: 2-5: 6-diepoxyhexane (I) is produced in good yield (80 per cent).</description><subject>Humanities and Social Sciences</subject><subject>letter</subject><subject>multidisciplinary</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1949</creationdate><recordtype>article</recordtype><recordid>eNptz09Lw0AQBfBFFIxV8BNIjnqIzv7JZnOU1qpQ8GDvYbOd1ZQkK5OkkG9vJBYvnuYwPx7vMXbN4Z6DNA9cKwWihBMWcZXpRGmTnbIIQJgEjNTn7KLr9gCQ8kxFTK8DNbavQhsHH9t4iz3Zz3FHwQ9k23iFVB2m_wFjT6GJV5Wt67G-ZGfe1h1e_d4Fe18_bZcvyebt-XX5uEmcMKpPSmVSkUvNRe5zrYU1iIKrXGfO-UwAokahMZXA09TtuDW8lE5IDm6qJxfsdk51FLqO0BdfVDWWxoJD8bO2OK6d6N1Mu4m0H0jFPgzUTt3-szezbW0_EP6FHsE3_NJc0w</recordid><startdate>19490903</startdate><enddate>19490903</enddate><creator>WOOD, D. J. C</creator><creator>WIGGINS, L. F</creator><general>Nature Publishing Group UK</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19490903</creationdate><title>Formation of a Tetrahydrofuran Derivative from Diallyl</title><author>WOOD, D. J. C ; WIGGINS, L. F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c284t-b4852936129f9662a8ee214967ccf720ee6e26e530155cd1a81b3c2310c5173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1949</creationdate><topic>Humanities and Social Sciences</topic><topic>letter</topic><topic>multidisciplinary</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WOOD, D. J. C</creatorcontrib><creatorcontrib>WIGGINS, L. F</creatorcontrib><collection>CrossRef</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WOOD, D. J. C</au><au>WIGGINS, L. F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Formation of a Tetrahydrofuran Derivative from Diallyl</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><date>1949-09-03</date><risdate>1949</risdate><volume>164</volume><issue>4166</issue><spage>402</spage><epage>403</epage><pages>402-403</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><abstract>WHEN diallyl (hexa-1: 5-diene) is treated with perbenzoic acid, 1: 2-5: 6-diepoxyhexane (I) is produced in good yield (80 per cent).</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><doi>10.1038/164402b0</doi><tpages>2</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-0836 |
ispartof | Nature (London), 1949-09, Vol.164 (4166), p.402-403 |
issn | 0028-0836 1476-4687 |
language | eng |
recordid | cdi_crossref_primary_10_1038_164402b0 |
source | Nature; SpringerLink Journals - AutoHoldings |
subjects | Humanities and Social Sciences letter multidisciplinary Science Science (multidisciplinary) |
title | Formation of a Tetrahydrofuran Derivative from Diallyl |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T16%3A32%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-nature_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Formation%20of%20a%20Tetrahydrofuran%20Derivative%20from%20Diallyl&rft.jtitle=Nature%20(London)&rft.au=WOOD,%20D.%20J.%20C&rft.date=1949-09-03&rft.volume=164&rft.issue=4166&rft.spage=402&rft.epage=403&rft.pages=402-403&rft.issn=0028-0836&rft.eissn=1476-4687&rft_id=info:doi/10.1038/164402b0&rft_dat=%3Cnature_cross%3E164402b0%3C/nature_cross%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 |