Functionalization at the double bond region of jojoba oil. 6. Production of amines via azides

Functionalization at the double bond region of jojoba oil. 6. Production of amines via azides

The apolar and hydrophobic jojoba molecule was made more hydrophilic by the incorporation of primary amino groups via the introduction and subsequent reduction of azido groups. The azides were obtained by the substitution of bromine or a mesylate group introduced into the jojoba oil molecule; by ope...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the American Oil Chemists' Society 1994-09, Vol.71 (9), p.993-997
Hauptverfasser: Avidon, Victor, Shani, Arnon
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 997
container_issue 9
container_start_page 993
container_title Journal of the American Oil Chemists' Society
container_volume 71
creator Avidon, Victor
Shani, Arnon
description The apolar and hydrophobic jojoba molecule was made more hydrophilic by the incorporation of primary amino groups via the introduction and subsequent reduction of azido groups. The azides were obtained by the substitution of bromine or a mesylate group introduced into the jojoba oil molecule; by opening of the epoxide ring in epoxy jojoba; or by the addition of bromoazide to the double bonds of jojoba.
doi_str_mv 10.1007/BF02542267
format Article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1007_BF02542267</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1007_BF02542267</sourcerecordid><originalsourceid>FETCH-LOGICAL-c229t-3136257bba065ff92e96619425f3d55497b13ed1d29069d56e7e92bf2e5647483</originalsourceid><addsrcrecordid>eNpFkMFKxDAYhIMoWFcvPkHOQmvyp0mboy52FRb0oOBFStIkmtJtJGkF9-m1KniaGT5mDoPQOSUFJaS6vG4I8BJAVAcoo5zXuWSMHqKMEMJyAvT5GJ2k1H_HmgHP0Eszj93kw6gGv1eLwWrC05vFJsx6sFiH0eBoXxcSHO5DH7TCwQ8FFgV-iMHMP_0Fqp0fbcIfXmG198amU3Tk1JDs2Z-u0FNz87i-zbf3m7v11TbvAOSUM8oE8EprRQR3ToKVQlBZAnfMcF7KSlNmDTUgiZCGC1tZCdqB5aKsypqt0MXvbhdDStG69j36nYqfLSXtckz7fwz7ArS8VHE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Functionalization at the double bond region of jojoba oil. 6. Production of amines via azides</title><source>SpringerNature Journals</source><creator>Avidon, Victor ; Shani, Arnon</creator><creatorcontrib>Avidon, Victor ; Shani, Arnon</creatorcontrib><description>The apolar and hydrophobic jojoba molecule was made more hydrophilic by the incorporation of primary amino groups via the introduction and subsequent reduction of azido groups. The azides were obtained by the substitution of bromine or a mesylate group introduced into the jojoba oil molecule; by opening of the epoxide ring in epoxy jojoba; or by the addition of bromoazide to the double bonds of jojoba.</description><identifier>ISSN: 0003-021X</identifier><identifier>EISSN: 1558-9331</identifier><identifier>DOI: 10.1007/BF02542267</identifier><language>eng</language><ispartof>Journal of the American Oil Chemists' Society, 1994-09, Vol.71 (9), p.993-997</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c229t-3136257bba065ff92e96619425f3d55497b13ed1d29069d56e7e92bf2e5647483</citedby><cites>FETCH-LOGICAL-c229t-3136257bba065ff92e96619425f3d55497b13ed1d29069d56e7e92bf2e5647483</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Avidon, Victor</creatorcontrib><creatorcontrib>Shani, Arnon</creatorcontrib><title>Functionalization at the double bond region of jojoba oil. 6. Production of amines via azides</title><title>Journal of the American Oil Chemists' Society</title><description>The apolar and hydrophobic jojoba molecule was made more hydrophilic by the incorporation of primary amino groups via the introduction and subsequent reduction of azido groups. The azides were obtained by the substitution of bromine or a mesylate group introduced into the jojoba oil molecule; by opening of the epoxide ring in epoxy jojoba; or by the addition of bromoazide to the double bonds of jojoba.</description><issn>0003-021X</issn><issn>1558-9331</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNpFkMFKxDAYhIMoWFcvPkHOQmvyp0mboy52FRb0oOBFStIkmtJtJGkF9-m1KniaGT5mDoPQOSUFJaS6vG4I8BJAVAcoo5zXuWSMHqKMEMJyAvT5GJ2k1H_HmgHP0Eszj93kw6gGv1eLwWrC05vFJsx6sFiH0eBoXxcSHO5DH7TCwQ8FFgV-iMHMP_0Fqp0fbcIfXmG198amU3Tk1JDs2Z-u0FNz87i-zbf3m7v11TbvAOSUM8oE8EprRQR3ToKVQlBZAnfMcF7KSlNmDTUgiZCGC1tZCdqB5aKsypqt0MXvbhdDStG69j36nYqfLSXtckz7fwz7ArS8VHE</recordid><startdate>199409</startdate><enddate>199409</enddate><creator>Avidon, Victor</creator><creator>Shani, Arnon</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199409</creationdate><title>Functionalization at the double bond region of jojoba oil. 6. Production of amines via azides</title><author>Avidon, Victor ; Shani, Arnon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c229t-3136257bba065ff92e96619425f3d55497b13ed1d29069d56e7e92bf2e5647483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Avidon, Victor</creatorcontrib><creatorcontrib>Shani, Arnon</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of the American Oil Chemists' Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Avidon, Victor</au><au>Shani, Arnon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functionalization at the double bond region of jojoba oil. 6. Production of amines via azides</atitle><jtitle>Journal of the American Oil Chemists' Society</jtitle><date>1994-09</date><risdate>1994</risdate><volume>71</volume><issue>9</issue><spage>993</spage><epage>997</epage><pages>993-997</pages><issn>0003-021X</issn><eissn>1558-9331</eissn><abstract>The apolar and hydrophobic jojoba molecule was made more hydrophilic by the incorporation of primary amino groups via the introduction and subsequent reduction of azido groups. The azides were obtained by the substitution of bromine or a mesylate group introduced into the jojoba oil molecule; by opening of the epoxide ring in epoxy jojoba; or by the addition of bromoazide to the double bonds of jojoba.</abstract><doi>10.1007/BF02542267</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0003-021X
ispartof Journal of the American Oil Chemists' Society, 1994-09, Vol.71 (9), p.993-997
issn 0003-021X
1558-9331
language eng
recordid cdi_crossref_primary_10_1007_BF02542267
source SpringerNature Journals
title Functionalization at the double bond region of jojoba oil. 6. Production of amines via azides
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T14%3A11%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Functionalization%20at%20the%20double%20bond%20region%20of%20jojoba%20oil.%206.%20Production%20of%20amines%20via%20azides&rft.jtitle=Journal%20of%20the%20American%20Oil%20Chemists'%20Society&rft.au=Avidon,%20Victor&rft.date=1994-09&rft.volume=71&rft.issue=9&rft.spage=993&rft.epage=997&rft.pages=993-997&rft.issn=0003-021X&rft.eissn=1558-9331&rft_id=info:doi/10.1007/BF02542267&rft_dat=%3Ccrossref%3E10_1007_BF02542267%3C/crossref%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